FDA Inspection 665977 — Richard Wolf GmbH

Richard Wolf GmbH — FEI 3002808001

The FDA completed an inspection of Richard Wolf GmbH on June 10, 2010 in Knittlingen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 10, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Knittlingen (Germany)

Citations

IDCFRDescription
331321 CFR 820.120(d)Records, DHR {see also 820.184(e)}