FDA Inspection 1260661 — EUROAPI FRANCE

EUROAPI FRANCE — FEI 1463

The FDA completed an inspection of EUROAPI FRANCE on Mar 8, 2024 in Vertolaye. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Mar 8, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vertolaye (France)

Additional details

Mutual Recognition Agreement (MRA)

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