# Bio Protech, Inc. – FDA Inspection, Dec 9, 2010

Source: https://www.keypedia.com/records/fda_inspections/bio-protech-inc/57b6546f-2b2e-4501-b2e0-b3a80ba4e4b0
Source feed: FDA_Inspections

> FDA inspection 704336 of Bio Protech, Inc., December 09, 2010. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 704336
- Company Name: Bio Protech, Inc.
- Inspection Date: 2010-12-09
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1318198 - 2026-04-09](https://www.keypedia.com/records/fda_inspections/bio-protech-inc/0b641380-81ac-481c-b13a-5eb41add8c69)
- FDA Inspection 977719 - 2016-03-23

Company: https://www.keypedia.com/companies/bio-protech-inc/6be640bc-59c4-4c6d-aa5b-a4c13a1e99f9

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