FDA Inspection 925317 — K+S France

K+S France — FEI 3004791302

The FDA completed an inspection of K+S France on April 17, 2015 in Dombasle Sur Meurthe. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 17, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dombasle Sur Meurthe (France)