FDA Inspection 1071829 — JW North America, Inc.

JW North America, Inc. — FEI 1000110800

The FDA completed an inspection of JW North America, Inc. on Nov 15, 2018 in cartersville, GA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 15, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
cartersville, GA (United States)

Citations

IDCFRDescription
504321 CFR 1010.3(a)(1)ID label lacks name and address

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