FDA Inspection
Kent Laboratories, Inc.Kent Laboratories, Inc. – FDA Inspection, Dec 7, 2016
Record Details
This FDA Inspection record concerns Kent Laboratories, Inc., with an inspection on December 7, 2016, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d2ccd1e8-ab33-47b7-8594-54b1c620c0ec
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 994520
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Kent Laboratories, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| July 28, 2026 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 14, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 21, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Kent Laboratories, Inc.
- FDA Inspection 1328290 - 2026-07-28
- FDA Inspection 807178 - 2012-11-14
- FDA Inspection 683180 - 2010-09-21
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