FDA Inspection 1083834 — Budelpack Poortvliet B.V.

Budelpack Poortvliet B.V. — FEI 3012872786

The FDA completed an inspection of Budelpack Poortvliet B.V. on Dec 19, 2018 in Poortvliet. 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
Dec 19, 2018
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Poortvliet (Netherlands)

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