# Hyperox Inc – FDA Inspection, Jan 28, 2009

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

> FDA inspection 643381 of Hyperox Inc, January 28, 2009. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

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
