FDA Inspection
Jensen Industries, Inc.Jensen Industries, Inc. – FDA Inspection, Mar 21, 2017
Record Details
This FDA Inspection record concerns Jensen Industries, Inc., with an inspection on March 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 28194eb6-b8fb-44be-840b-db0cc5b86fe7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1006004
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Jensen Industries, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 9, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 3, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Jensen Industries, Inc.
- FDA Inspection 831783 - 2013-05-09
- FDA Inspection 611027 - 2009-09-03
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