FDA Inspection 896070 — Richard Wolf GmbH

Richard Wolf GmbH — FEI 3002808001

The FDA completed an inspection of Richard Wolf GmbH on August 29, 2014 in Knittlingen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 29, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Knittlingen (Germany)