FDA Inspection 1093157 — NextPharma Ploermel

NextPharma Ploermel — FEI 3004298189

The FDA completed an inspection of NextPharma Ploermel on Apr 20, 2018 in Ploermel. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 20, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ploermel (France)

Additional Details

Mutual Recognition Agreement (MRA)