Panchmahal Dist. Co-Operative Milk Producer Union Ltd.
FDA import alert and refusal historyGodhra, IndiaFEI 3003166393
Recorded by FDA as PANCHMAHAL DIST. CO-OPERATIVE MILK PRODUCER UNION LTD.
As of October 26, 2026, Panchmahal Dist. Co-Operative Milk Producer Union Ltd. (GODHRA, India) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for amul pure ghee, published by FDA on June 1, 2020, 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 99-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Panchmahal Dist. Co-Operative Milk Producer Union Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2020
- Import alert listingListed on Import Alert 99-39red listAmul pure gheeSource
Questions about Panchmahal Dist. Co-Operative Milk Producer Union Ltd.
- Is Panchmahal Dist. Co-Operative Milk Producer Union Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Panchmahal Dist. Co-Operative Milk Producer Union Ltd. is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for amul pure ghee; FDA published the listing on June 1, 2020.
- Has FDA refused shipments from Panchmahal Dist. Co-Operative Milk Producer Union Ltd.?
- No FDA import refusals for Panchmahal Dist. Co-Operative Milk Producer Union Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Panchmahal Dist. Co-Operative Milk Producer Union Ltd.'s FEI number?
- Panchmahal Dist. Co-Operative Milk Producer Union Ltd.'s FDA Establishment Identifier (FEI) is 3003166393.
- Can shipments from Panchmahal Dist. Co-Operative Milk Producer Union Ltd. still enter the U.S.?
- Shipments of amul pure ghee from Panchmahal Dist. Co-Operative Milk Producer Union Ltd. can be detained without physical examination under Import Alert 99-39; 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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