FDA Inspection 634581 — Olympus Winter & IBE Gmbh

Olympus Winter & IBE Gmbh — FEI 3002807798

The FDA completed an inspection of Olympus Winter & IBE Gmbh on Dec 3, 2009 in Hamburg. 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
Dec 3, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Hamburg (Germany)