# FDA Inspection 1118468 - Bio Protech Usa, Inc. - February 20, 2020

Source: https://www.keypedia.com/records/fda_inspections/bio-protech-usa-inc/47b178cd-b3f3-4c23-9ca9-e44bb6d524d5
Source feed: FDA_Inspections

> FDA Inspection 1118468 for Bio Protech Usa, Inc. on February 20, 2020. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1118468
- Company Name: Bio Protech Usa, Inc.
- Inspection Date: 2020-02-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1118468 - 2020-02-20](https://www.keypedia.com/records/fda_inspections/bio-protech-usa-inc/4ced4dc9-18fa-41c3-abb2-cb73bc50cae9)
- [FDA Inspection 872425 - 2014-02-26](https://www.keypedia.com/records/fda_inspections/bio-protech-usa-inc/023a538c-f56e-45f9-a1db-7db7360ba895)
- [FDA Inspection 872425 - 2014-02-26](https://www.keypedia.com/records/fda_inspections/bio-protech-usa-inc/fd994349-f0f6-4f31-9c03-70f7e11876f5)
- [FDA Inspection 742473 - 2011-08-31](https://www.keypedia.com/records/fda_inspections/bio-protech-usa-inc/bc64112a-a82c-474a-9e65-bad8f655bcc2)

Company: https://www.keypedia.com/companies/bio-protech-usa-inc/2b82abd2-b0da-4769-b1f4-fd7a5203f8d3

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