FDA Inspection 1222114 — Haupt Pharma Muenster GmbH

Haupt Pharma Muenster GmbH — FEI 3006010798

The FDA completed an inspection of Haupt Pharma Muenster GmbH on Nov 24, 2021 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
Nov 24, 2021
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Munster (Germany)

Additional Details

Mutual Recognition Agreement (MRA)