# Kinetic Instruments, Inc. – FDA Inspection, Jan 6, 2016

Source: https://www.keypedia.com/records/fda_inspections/kinetic-instruments-inc/c22f1f78-8f83-4356-86a3-779b563f6500
Source feed: FDA_Inspections

> FDA inspection 955255 of Kinetic Instruments, Inc., January 06, 2016. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 955255
- Company Name: Kinetic Instruments, Inc.
- Inspection Date: 2016-01-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1100800 - 2019-08-14

Company: https://www.keypedia.com/companies/kinetic-instruments-inc/8a923a2a-81a5-46d7-9013-4dd81f384187

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