FDA Inspection 1235010 — Delpharm Tours

Delpharm Tours — FEI 3008349307

The FDA completed an inspection of Delpharm Tours on June 11, 2021 in Chambray Les Tours. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 11, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Chambray Les Tours (France)

Additional Details

Mutual Recognition Agreement (MRA)