FDA Inspection 1305638 — Allphamed PHARBIL Arzneimittel GmbH

Allphamed PHARBIL Arzneimittel GmbH — FEI 3008587095

The FDA completed an inspection of Allphamed PHARBIL Arzneimittel GmbH on Nov 19, 2024 in Gottingen. 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
Nov 19, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gottingen (Germany)

Additional Details

Mutual Recognition Agreement (MRA)

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