Hong Kong Tianlong Technology International Group Company
FDA import alert and refusal historyMong Kok, Hong KongFEI 3009326649
As of October 27, 2026, Hong Kong Tianlong Technology International Group Company (Mong Kok, Hong Kong) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for france t253 tablets, published by FDA on May 15, 2015, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 54-16 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Hong Kong Tianlong Technology International Group Company
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 54-16red listFrance T253 TabletsSource
Questions about Hong Kong Tianlong Technology International Group Company
- Is Hong Kong Tianlong Technology International Group Company on an FDA import alert?
- Yes. As of October 27, 2026, Hong Kong Tianlong Technology International Group Company is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for france t253 tablets; FDA published the listing on May 15, 2015.
- Has FDA refused shipments from Hong Kong Tianlong Technology International Group Company?
- No FDA import refusals for Hong Kong Tianlong Technology International Group Company appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Hong Kong Tianlong Technology International Group Company's FEI number?
- Hong Kong Tianlong Technology International Group Company's FDA Establishment Identifier (FEI) is 3009326649.
- Can shipments from Hong Kong Tianlong Technology International Group Company still enter the U.S.?
- Shipments of france t253 tablets from Hong Kong Tianlong Technology International Group Company can be detained without physical examination under Import Alert 54-16; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.