# FDA Inspection 960670 - Air Kinetic Technologies Corp. - February 25, 2016

Source: https://www.keypedia.com/records/fda_inspections/air-kinetic-technologies-corp/48d68bcb-0b01-4d0d-bc7a-38db78257cb9
Source feed: FDA_Inspections

> FDA Inspection 960670 for Air Kinetic Technologies Corp. on February 25, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 960670
- Company Name: Air Kinetic Technologies Corp.
- Inspection Date: 2016-02-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 960670 - 2016-02-25](https://www.keypedia.com/records/fda_inspections/air-kinetic-technologies-corp/19f7146c-e4cd-4398-8289-40d69a9df688)

Company: https://www.keypedia.com/companies/air-kinetic-technologies-corp/e998e42b-6dfc-444e-8b3d-95cd94e62d84

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