FSVP supplier monitoring
Every foreign food supplier, checked against FDA import alerts every day and against refusals, warning letters, inspections and recalls every week. Look up any supplier free. Watch the ones you buy from.
Independent. Not affiliated with the U.S. FDA. Every fact links to its FDA source.
Sample Seafood Co., Ltd.
Ca Mau, Vietnam · FEI 1234567890
Last checked Oct 17, 2026
6 refusals since 2016
Your watchlist
Status, the last change and when each three-year reevaluation is due. When FDA publishes something new, the row opens with what changed and a link to the source.
Listed on Import Alert 16‑124 on Oct 16, 2026.
21 CFR 1.505(c)(1)
New information about this supplier. Reevaluate it promptly and document it.
Generate dated PDFIN · Refused, ground turmeric, Aug 2, 2026
MX · Removed, Import Alert 99-19, Oct 15, 2026
TH · Warning letter issued, Oct 14, 2026
KR · Inspection classified VAI, Jun 12, 2026
KR · No FDA records
| Supplier | Status | Last change | Next review |
|---|---|---|---|
Sample Seafood Co., Ltd.VN · FEI 1234567890 IA 16-124 · Red listListed on an import alertOct 16, 2026NewAs of Oct 17, 2026, Sample Seafood Co., Ltd. is on Import Alert 16‑124 (red list) since Oct 16, 2026, with 6 import refusals recorded since October 2016.
21 CFR 1.505(c)(1) New information about this supplier. Reevaluate it promptly and document the reevaluation. Generate dated PDFOpen record | |||
| Sample Spice Exports Pvt. Ltd.IN | No active alert | Refused, ground turmericAug 2, 2026 | Mar 2027 |
| Sample Foods S.A. de C.V.MX | Removed from IA 99-19 | Removed, Import Alert 99-19Oct 15, 2026 | Jan 2027 |
| Sample Agro Co., Ltd.TH | No active alert | Warning letter issuedOct 14, 2026 | Due now |
| Sample Nutrition Co.KR | No active alert | Inspection classified VAIJun 12, 2026 | Sep 2028 |
| Sample Noodle Co., Ltd.KR | No active alert | No FDA records | Feb 2029 |
The rule you already follow
What it asks of an importer
Before approving a foreign supplier, consider its FDA compliance record. When new information appears, reevaluate promptly and write it down. At least every three years, reevaluate anyway.
A summary, not legal advice. The text on the right is verbatim.
“…you must promptly reevaluate the concerns associated with the factors in paragraph (a)(1) of this section when you become aware of new information about these factors, and the reevaluation must be documented.”
21 CFR 1.505(c)(1)Read it on eCFR
The factors include
“whether the foreign supplier is the subject of an FDA warning letter, import alert, or other FDA compliance action related to food safety”
21 CFR 1.505(a)(1)(iii)(B)
SupplierRadar is how you become aware. The dated PDF is how you document it.
We check import alerts every day and the other FDA records every week. When a supplier you watch changes, you get the source and a one-page record for your FSVP file.
How it works
Search by name or FEI, or paste your list. One supplier is free; no card.
What changed, when FDA published it, and the link to the source. Never a score, never an opinion.
21 CFR 1.505(c)(1): reevaluate this supplier promptly and document it.
One page per supplier: what was checked, when, and where each fact came from. You add your decision and sign.
Foreign supplier evaluation record
Public FDA records checked Oct 17, 2026, 06:12 UTC 1
SAMPLE
Page 1 of 1
Sources checked 2
| Import alerts | data as of Oct 17, 2026 | Listed, 16-124 |
| Import refusals | data as of Oct 14, 2026 | 6 since 2016 |
| Warning letters | data as of Oct 14, 2026 | None on record |
| Inspection classifications | data as of Oct 14, 2026 | VAI, Jun 2023 |
| Recalls | data as of Oct 14, 2026 | None on record |
Importer's evaluation and decision
Pricing
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$133/ month, from
Entry price published on Registrar Corp's monitoring page (five facilities), checked October 2026. Full comparison
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Free tool
Paste names or FEI numbers, one per line. You get each supplier's current FDA status, with a link to its full record. No account needed. Open the full bulk check
Paste your list and press Check. Each supplier gets its import alert status, refusal count and a link to its full record. No account needed for up to 5.
Questions
No. SupplierRadar is an independent service that organizes public FDA records by supplier. It is not affiliated with or endorsed by the U.S. Food and Drug Administration, and every fact links to the FDA record it came from.
Import alert lists are checked every day. Import refusals, warning letters, inspection classifications and recalls are checked every week, which matches how often FDA updates them. Every page shows when it was last checked.
On Starter and above you get one email with what changed, the date FDA published it and a link to the source, plus a button to generate a dated PDF for your FSVP file. The Free plan includes a weekly summary.
No. It shows FDA's records with their dates and sources, without scores or recommendations. The evaluation and the decision stay with the importer, as 21 CFR 1.505 requires.
Anyone can request a correction from the supplier page. We check the request against the FDA source and reply by email, usually within 48 hours.
No. Watching one supplier is free, and the 14-day Starter trial does not ask for a card. Paid plans are billed through PayPal and can be cancelled from the billing page.
Built for the person who signs the FSVP file
Enter your work email and we send a sign-in link. No password, no card. Add the rest of your suppliers when you are ready.
