FDA Inspection 601626 — Pharmpur Gmbh

Pharmpur Gmbh — FEI 3005689226

The FDA completed an inspection of Pharmpur Gmbh on Jul 16, 2009 in Konigsbrunn. 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 16, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Konigsbrunn (Germany)

Additional Details

Postmarket Audit Inspections