FDA Inspection 1133484 — Haupt Pharma Wolfratshausen GmbH

Haupt Pharma Wolfratshausen GmbH — FEI 3000310230

The FDA completed an inspection of Haupt Pharma Wolfratshausen GmbH on Aug 5, 2020 in Wolfratshausen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 5, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wolfratshausen (Germany)

Additional details

Mutual Recognition Agreement (MRA)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.