FDA Inspection 988740 — INKE S.A.

INKE S.A. — FEI 3003663245

The FDA completed an inspection of INKE S.A. on April 15, 2016 in Castellbisbal. 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 15, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Castellbisbal (Spain)