FDA Inspection 875515 — Katena Products Inc.

Katena Products Inc. — FEI 1051791

The FDA completed an inspection of Katena Products Inc. on Apr 21, 2014 in Saint Petersburg, FL. 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
Apr 21, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Saint Petersburg, FL (United States)