FDA Inspection
Katena Products, Inc.Katena Products, Inc. – FDA Inspection, Sep 20, 2018
Record Details
This FDA Inspection record concerns Katena Products, Inc., with an inspection on September 20, 2018, issued by the New Jersey District Office, covering medical devices & rad health.
- Company
- Katena Products, Inc.
- Inspection Date
- September 20, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · eb11c902-1539-4092-8413-25f334616577
Inspection Facts
- Inspection number
- 1123022
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
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 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 |
| February 22, 2012 | 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 1026619 - 2017-09-12
- FDA Inspection 986240 - 2016-08-31
- FDA Inspection 768294 - 2012-02-22
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