# FDA Inspection 1201529 - AirScan Inc. d/b/a HemaTechnologies - March 24, 2023

Source: https://www.keypedia.com/records/fda_inspections/airscan-inc-dba-hematechnologies/294f63d4-62eb-4074-a35e-5ba825bb7d0a
Source feed: FDA_Inspections

> FDA Inspection 1201529 for AirScan Inc. d/b/a HemaTechnologies on March 24, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1201529
- Company Name: AirScan Inc. d/b/a HemaTechnologies
- Inspection Date: 2023-03-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1201529 - 2023-03-24](https://www.keypedia.com/records/fda_inspections/airscan-inc-dba-hematechnologies/c4be87e9-cdf7-47cc-85a9-ba05eebbfe8c)

Company: https://www.keypedia.com/companies/airscan-inc-dba-hematechnologies/9a63713a-2f50-47ba-a5c8-80aed7405435

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