FDA Inspection 1098838 — Owen Mumford USA, Inc.

Owen Mumford USA, Inc. — FEI 1000219614

The FDA completed an inspection of Owen Mumford USA, Inc. on Mar 5, 2019 in Marietta, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 5, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Marietta, GA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.