FDA Inspection 875643 — Haupt Pharma Muenster GmbH

Haupt Pharma Muenster GmbH — FEI 3006010798

The FDA completed an inspection of Haupt Pharma Muenster GmbH on Mar 21, 2014 in Munster. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 21, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Munster (Germany)