Pk Bas
FDA import alert and refusal historySchenefeld, GermanyFEI 3013545498
Recorded by FDA as PK BAS
As of October 26, 2026, Pk Bas is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between July 3, 2017 and July 13, 2017, most often for fair packaging and labeling act (LABELING).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Other formula products, n.e.c., powder formula · LABELING
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Pk Bas
3 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Other formula products, n.e.c., powder formulaLABELINGEntry AEK-3604486-2Source
- Import refusalRefused, Milk base infant formula product (0-12 months), powder formulaLABELINGEntry AEK-3588848-3Source
- Import refusalRefused, Milk base infant formula product (0-12 months), powder formulaLABELINGEntry AEK-3588858-2Source
Refusal charges, in plain English
- LABELING3 refused lines
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
Questions about Pk Bas
- Is Pk Bas on an FDA import alert?
- No listing for Pk Bas appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Germany page.
- Has FDA refused shipments from Pk Bas?
- Yes. FDA refused 3 shipment lines from Pk Bas between July 3, 2017 and July 13, 2017. The most recent, on July 13, 2017, was other formula products, n.e.c., powder formula, charged as LABELING (fair packaging and labeling act).
- Why did FDA refuse Pk Bas's shipments?
- The most frequent charge is LABELING (fair packaging and labeling act, 3 lines).
- What is Pk Bas's FEI number?
- Pk Bas's FDA Establishment Identifier (FEI) is 3013545498.
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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.