FDA Inspection 1198730 — Richard Wolf GmbH

Richard Wolf GmbH — FEI 3002808001

The FDA completed an inspection of Richard Wolf GmbH on October 20, 2022 in Knittlingen. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
October 20, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Knittlingen (Germany)