FDA Inspection 650243 — NextPharma Ploermel

NextPharma Ploermel — FEI 3004298189

The FDA completed an inspection of NextPharma Ploermel on Feb 17, 2010 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
Feb 17, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ploermel (France)