# FDA Inspection 643381 - Hyperox Inc - January 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/hyperox-inc/79bb9a77-6b8a-4c95-84a6-18f5e5bc1862
Source feed: FDA_Inspections

> FDA Inspection 643381 for Hyperox Inc on January 28, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 643381
- Company Name: Hyperox Inc
- Inspection Date: 2009-01-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 643381 - 2009-01-28](https://www.keypedia.com/records/fda_inspections/hyperox-inc/65916ca3-a7af-4b0a-8b83-6a9649bb997c)

Company: https://www.keypedia.com/companies/hyperox-inc/d843d9b5-5d52-43bc-9749-1d6543ea1208

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