FDA Inspection
Katena Products, Inc.Katena Products, Inc. – FDA Inspection, Nov 9, 2009
Record Details
This FDA Inspection record concerns Katena Products, Inc., with an inspection on November 9, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Katena Products, Inc.
- Inspection Date
- November 9, 2009
- Product Type
- Devices
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ID · dba320d2-0123-4fad-b0fd-bb0358df0f54
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 629009
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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Other FDA inspections of Katena Products, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| March 1, 2024 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| January 6, 2020 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| September 20, 2018 | Not classified | New Jersey District Office | |
| September 12, 2017 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| August 31, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Katena Products, Inc.
- FDA Inspection 1234623 - 2024-03-01
- FDA Inspection 1114594 - 2020-01-06
- FDA Inspection 1123022 - 2018-09-20
- FDA Inspection 1026619 - 2017-09-12
- FDA Inspection 986240 - 2016-08-31
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