FDA Inspection 1098838 — Owen Mumford USA, Inc.

Owen Mumford USA, Inc. — FEI 1000219614

The FDA completed an inspection of Owen Mumford USA, Inc. on March 5, 2019 in Marietta, GA. 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
March 5, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Marietta, GA (United States)