# Kent Laboratories, Inc. – FDA Inspection, Dec 7, 2016

Source: https://www.keypedia.com/records/fda_inspections/kent-laboratories-inc/d2ccd1e8-ab33-47b7-8594-54b1c620c0ec
Source feed: FDA_Inspections

> FDA inspection 994520 of Kent Laboratories, Inc., December 07, 2016. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 994520
- Company Name: Kent Laboratories, Inc.
- Inspection Date: 2016-12-07
- 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: 0

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- [FDA Inspection 1328290 - 2026-07-28](https://www.keypedia.com/records/fda_inspections/kent-laboratories-inc/5da66d00-e439-4d7b-b81a-a0f8cf448296)
- FDA Inspection 807178 - 2012-11-14
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## Related Officers

- [Company Rep](https://www.keypedia.com/people/paul-m-kawamoto/0a24b110-12de-4736-8d98-7a023ceec01e)

Company: https://www.keypedia.com/companies/kent-laboratories-inc/14a4dc50-b267-4fed-91a9-84490accd72f

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