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FDA Inspection 630664 — K.W. Griffen Company

K.W. Griffen Company — FEI 1211177

The FDA completed an inspection of K.W. Griffen Company on November 9, 2009 in Norwalk, CT. 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
November 9, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Norwalk, CT (United States)

Facility

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