FDA Inspection 632743 — Kerr Corporation

Kerr Corporation — FEI 2024312

The FDA completed an inspection of Kerr Corporation on Dec 7, 2009 in Orange, CA. 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
Dec 7, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Orange, CA (United States)

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