FDA Inspection 1181729 — K+S France

K+S France — FEI 3004791302

The FDA completed an inspection of K+S France on September 22, 2021 in Dombasle Sur Meurthe. 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
September 22, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dombasle Sur Meurthe (France)

Additional Details

Mutual Recognition Agreement (MRA)