# FDA Inspection 955255 - Kinetic Instruments, Inc. - January 06, 2016

Source: https://www.keypedia.com/records/fda_inspections/kinetic-instruments-inc/a60960b2-7727-4aca-8857-aed28d81029b
Source feed: FDA_Inspections

> FDA Inspection 955255 for Kinetic Instruments, Inc. on January 06, 2016. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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