# Katena Products, Inc. – FDA Inspection, Nov 9, 2009

Source: https://www.keypedia.com/records/fda_inspections/katena-products-inc/dba320d2-0123-4fad-b0fd-bb0358df0f54
Source feed: FDA_Inspections

> FDA inspection 629009 of Katena Products, Inc., November 09, 2009. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 629009
- Company Name: Katena Products, Inc.
- Inspection Date: 2009-11-09
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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Company: https://www.keypedia.com/companies/katena-products-inc/263ef7d5-d73c-4f31-8090-95297c342713

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7