Zaklad Produkcyjny Bakoma S.A
FDA import alert and refusal historySzymanow, PolandFEI 3003805918
As of October 26, 2026, Zaklad Produkcyjny Bakoma S.A has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on January 20, 2017, was classified NAI (No Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Zaklad Produkcyjny Bakoma S.A
2 records, newest first. Each line links to the FDA page it came from.
Questions about Zaklad Produkcyjny Bakoma S.A
- Is Zaklad Produkcyjny Bakoma S.A on an FDA import alert?
- No listing for Zaklad Produkcyjny Bakoma S.A appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Poland page.
- Has FDA refused shipments from Zaklad Produkcyjny Bakoma S.A?
- No FDA import refusals for Zaklad Produkcyjny Bakoma S.A appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Zaklad Produkcyjny Bakoma S.A last inspected by FDA?
- FDA's most recent inspection of Zaklad Produkcyjny Bakoma S.A with a final classification is dated January 20, 2017 and was classified NAI (No Action Indicated).
- What is Zaklad Produkcyjny Bakoma S.A's FEI number?
- Zaklad Produkcyjny Bakoma S.A's FDA Establishment Identifier (FEI) is 3003805918.
Buying from Zaklad Produkcyjny Bakoma S.A?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.