# FDA Inspection 737564 - O-Two Medical Technologies, Inc. - August 04, 2011

Source: https://www.keypedia.com/records/fda_inspections/o-two-medical-technologies-inc/00bf11e5-c533-4696-b8a2-a6d65b543dce
Source feed: FDA_Inspections

> FDA Inspection 737564 for O-Two Medical Technologies, Inc. on August 04, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 737564
- Company Name: O-Two Medical Technologies, Inc.
- Inspection Date: 2011-08-04
- 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 737564 - 2011-08-04](https://www.keypedia.com/records/fda_inspections/o-two-medical-technologies-inc/9f95ca7d-0056-4896-9ff4-a977b2b69565)
- [FDA Inspection 553077 - 2008-12-11](https://www.keypedia.com/records/fda_inspections/o-two-medical-technologies-inc/90445255-5f94-466e-b294-ecb80d83c489)

Company: https://www.keypedia.com/companies/o-two-medical-technologies-inc/6188acdb-b2a6-4f09-9fb1-5d6c71353559

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