FDA Inspection 894011 — Allphamed PHARBIL Arzneimittel GmbH

Allphamed PHARBIL Arzneimittel GmbH — FEI 3008587095

The FDA completed an inspection of Allphamed PHARBIL Arzneimittel GmbH on Sep 5, 2014 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
Sep 5, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gottingen (Germany)

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