# FDA Inspection 621402 - AirSep Corp. - October 05, 2009

Source: https://www.keypedia.com/records/fda_inspections/airsep-corp/87ce3a63-6b62-4b2e-a911-2d629cbf7f63
Source feed: FDA_Inspections

> FDA Inspection 621402 for AirSep Corp. on October 05, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 621402
- Company Name: AirSep Corp.
- Inspection Date: 2009-10-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 731958 - 2011-06-29](https://www.keypedia.com/records/fda_inspections/airsep-corp/e6d6e0d6-0195-4757-b0de-a20327eaaf4d)
- [FDA Inspection 621402 - 2009-10-05](https://www.keypedia.com/records/fda_inspections/airsep-corp/f5a94619-6cf6-412b-99c6-dfb726cfdc78)

Company: https://www.keypedia.com/companies/airsep-corp/2acff99b-f8bb-4543-8bdf-4b5280db3063

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