Ak 91
FDA import alert and refusal historyBangkok, ThailandFEI 3013680935
Recorded by FDA as AK 91
As of October 26, 2026, Ak 91 is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 22, 2017, most often for no u.s. adverse event contact on supplement label (NCONTACT).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Dietary conventional foods, n.e.c. · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ak 91
1 record, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Dietary conventional foods, n.e.c.NO ENGLISHNCONTACTEntry AEK-3725246-4Source
Refusal charges, in plain English
- NCONTACT1 refused line
No U.S. adverse event contact on supplement label
The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.
- NO ENGLISH1 refused line
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
Questions about Ak 91
- Is Ak 91 on an FDA import alert?
- No listing for Ak 91 appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Thailand page.
- Has FDA refused shipments from Ak 91?
- Yes. FDA refused 1 shipment line from Ak 91 on August 22, 2017. The most recent, on August 22, 2017, was dietary conventional foods, n.e.c., charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Ak 91's shipments?
- The most frequent charges are NCONTACT (no u.s. adverse event contact on supplement label, 1 line) and NO ENGLISH (required label information not in english, 1 line).
- What is Ak 91's FEI number?
- Ak 91's FDA Establishment Identifier (FEI) is 3013680935.
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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.