Atrey Pharmaceuticals Private Limited
FDA import alert and refusal historyGujarat, IndiaFEI 3021630215
Recorded by FDA as ATREY PHARMACEUTICALS PRIVATE LIMITED
As of October 26, 2026, Atrey Pharmaceuticals Private Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines between August 31, 2017 and September 24, 2025, most often for unapproved new drug (UNAPPROVED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Refined vegetable oil, single ingredient, n.e.c. · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Atrey Pharmaceuticals Private Limited
7 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 3 lines in one entry: Refined vegetable oil, single ingredient, n.e.c.UNAPPROVEDEntry KM6-3655493-3Show 3 linesHide lines
- Refused, Refined vegetable oil, single ingredient, n.e.c.UNAPPROVEDEntry KM6-3655493-3Source
- Refused, Refined vegetable oil, single ingredient, n.e.c.UNAPPROVEDEntry KM6-3655493-3Source
- Refused, Refined vegetable oil, single ingredient, n.e.c.UNAPPROVEDEntry KM6-3655493-3Source
2017
- Import refusalSource
Refused, 4 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NOT LISTEDUNAPPROVEDDIETARYLBLNCONTACTEntry UPS-4784020-3Show 4 linesHide lines
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NOT LISTEDUNAPPROVEDEntry UPS-4784020-3Source
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.DIETARYLBLNCONTACTEntry UPS-4784020-3Source
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.DIETARYLBLNCONTACTEntry UPS-4784020-3Source
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.DIETARYLBLNCONTACTEntry UPS-4784020-3Source
Refusal charges, in plain English
- UNAPPROVED4 refused lines
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
- DIETARYLBL3 refused lines
Not identified as a dietary supplement
The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).
- NCONTACT3 refused lines
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.
- NOT LISTED1 refused line
Product not listed with FDA
The product appeared to be a drug or device that is not included in the listing FDA requires under section 510(j) of the FD&C Act.
Questions about Atrey Pharmaceuticals Private Limited
- Is Atrey Pharmaceuticals Private Limited on an FDA import alert?
- No listing for Atrey Pharmaceuticals Private Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
- Has FDA refused shipments from Atrey Pharmaceuticals Private Limited?
- Yes. FDA refused 7 shipment lines from Atrey Pharmaceuticals Private Limited between August 31, 2017 and September 24, 2025. The most recent, on September 24, 2025, was refined vegetable oil, single ingredient, n.e.c., charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Atrey Pharmaceuticals Private Limited's shipments?
- The most frequent charges are UNAPPROVED (unapproved new drug, 4 lines) and DIETARYLBL (not identified as a dietary supplement, 3 lines).
- What is Atrey Pharmaceuticals Private Limited's FEI number?
- Atrey Pharmaceuticals Private Limited's FDA Establishment Identifier (FEI) is 3021630215.
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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.