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FDA Inspection 1009115 — George Taub Products & Fusion Co., Inc.

George Taub Products & Fusion Co., Inc. — FEI 2241860

The FDA completed an inspection of George Taub Products & Fusion Co., Inc. on April 18, 2017 in Jersey City, NJ. 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
April 18, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Jersey City, NJ (United States)

Facility

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FDA data resources