FDA Inspection 748525 — Pharmpur Gmbh

Pharmpur Gmbh — FEI 3005689226

The FDA completed an inspection of Pharmpur Gmbh on Sep 13, 2011 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
Sep 13, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Konigsbrunn (Germany)