# FDA Inspection 816798 - Bio-Med U.S.A., Inc. - January 23, 2013

Source: https://www.keypedia.com/records/fda_inspections/bio-med-usa-inc/7ea88cd0-4518-458c-8658-a0ea9098f0ce
Source feed: FDA_Inspections

> FDA Inspection 816798 for Bio-Med U.S.A., Inc. on January 23, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 816798
- Company Name: Bio-Med U.S.A., Inc.
- Inspection Date: 2013-01-23
- 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 816798 - 2013-01-23](https://www.keypedia.com/records/fda_inspections/bio-med-usa-inc/43c5f3c2-7b11-4b90-a54a-616aad6089e1)
- [FDA Inspection 672514 - 2010-07-19](https://www.keypedia.com/records/fda_inspections/bio-med-usa-inc/045365dd-1471-411c-84a7-02ec8beeb3c4)
- [FDA Inspection 672514 - 2010-07-19](https://www.keypedia.com/records/fda_inspections/bio-med-usa-inc/48d50609-b5bf-4709-957b-a37104b88913)

Company: https://www.keypedia.com/companies/bio-med-usa-inc/71f22d1b-0562-470c-a782-552e533afd55

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