FDA Inspection 1282122 — Ambipack B.V.

Ambipack B.V. — FEI 3018007593

The FDA completed an inspection of Ambipack B.V. on Aug 27, 2025 in Hendrik-Ido-Ambacht. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 27, 2025
Fiscal Year
2025
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Hendrik-Ido-Ambacht (Netherlands)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.