FDA Inspection 1056600 — GWR Medical, Inc.

GWR Medical, Inc. — FEI 3008847017

The FDA completed an inspection of GWR Medical, Inc. on May 14, 2018 in Chadds Ford, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 14, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Chadds Ford, PA (United States)