FDA Inspection 945384 — Balkanpharma Dupnitsa AD

Balkanpharma Dupnitsa AD — FEI 3009526337

The FDA completed an inspection of Balkanpharma Dupnitsa AD on August 28, 2015 in Dupnitsa. 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
August 28, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dupnitsa (Bulgaria)