FDA Inspection 1031326 — JW North America, Inc.

JW North America, Inc. — FEI 1000110800

The FDA completed an inspection of JW North America, Inc. on Oct 25, 2017 in cartersville, 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
Oct 25, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
cartersville, GA (United States)

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