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FDA Inspection 768294 — Katena Products, Inc.

Katena Products, Inc. — FEI 2242450

The FDA completed an inspection of Katena Products, Inc. on February 22, 2012 in Randolph, 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
February 22, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Randolph, NJ (United States)

Facility

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FDA data resources