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FDA Inspection 1125617 — Delpharm Huningue S.A.S.

Delpharm Huningue S.A.S. — FEI 3003157245

The FDA completed an inspection of Delpharm Huningue S.A.S. on August 8, 2019 in Huningue. 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
August 8, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Huningue (France)

Additional Details

Mutual Recognition Agreement (MRA)

Facility

Other inspections at this facility

  • 1262708 (VAI Thu Nov 30 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1060634 (NAI Fri Jun 22 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 988001 (NAI Fri Sep 23 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 913598 (NAI Fri Dec 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 765433 (VAI Thu Dec 15 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources