The Pure Goat Company
FDA import alert and refusal historyAmsterdam, NetherlandsFEI 3027181242
Recorded by FDA as THE PURE GOAT COMPANY
As of October 26, 2026, The Pure Goat Company is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on July 18, 2023, most often for required label information not in english (NO ENGLISH).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Milk base infant formula product (0-12 months), powder formula · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for The Pure Goat Company
1 record, newest first. Each line links to the FDA page it came from.
2023
- Import refusalRefused, Milk base infant formula product (0-12 months), powder formulaNO ENGLISHEntry SCS-7169540-0Source
Refusal charges, in plain English
- 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 The Pure Goat Company
- Is The Pure Goat Company on an FDA import alert?
- No listing for The Pure Goat Company appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Netherlands page.
- Has FDA refused shipments from The Pure Goat Company?
- Yes. FDA refused 1 shipment line from The Pure Goat Company on July 18, 2023. The most recent, on July 18, 2023, was milk base infant formula product (0-12 months), powder formula, charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse The Pure Goat Company's shipments?
- The most frequent charge is NO ENGLISH (required label information not in english, 1 line).
- What is The Pure Goat Company's FEI number?
- The Pure Goat Company's FDA Establishment Identifier (FEI) is 3027181242.
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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.