# FDA Inspection 1100800 - Kinetic Instruments, Inc. - August 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/kinetic-instruments-inc/7b61d261-221b-408a-bce0-785f0494d44d
Source feed: FDA_Inspections

> FDA Inspection 1100800 for Kinetic Instruments, Inc. on August 14, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100800
- Company Name: Kinetic Instruments, Inc.
- Inspection Date: 2019-08-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1100800 - 2019-08-14](https://www.keypedia.com/records/fda_inspections/kinetic-instruments-inc/74a14584-d1eb-4adf-bda1-4e3c48b584b0)
- [FDA Inspection 955255 - 2016-01-06](https://www.keypedia.com/records/fda_inspections/kinetic-instruments-inc/a60960b2-7727-4aca-8857-aed28d81029b)
- [FDA Inspection 955255 - 2016-01-06](https://www.keypedia.com/records/fda_inspections/kinetic-instruments-inc/c22f1f78-8f83-4356-86a3-779b563f6500)

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