# BioPro, Inc. – FDA Inspection, Feb 3, 2012

Source: https://www.keypedia.com/records/fda_inspections/biopro-inc/82810946-20b2-4bbd-921f-f90c6c33f271
Source feed: FDA_Inspections

> FDA inspection 766155 of BioPro, Inc., February 03, 2012. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 766155
- Company Name: BioPro, Inc.
- Inspection Date: 2012-02-03
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 947607 - 2015-10-07
- [FDA Inspection 904881 - 2014-11-25](https://www.keypedia.com/records/fda_inspections/biopro-inc/2cf225b3-11b0-48ec-ae1e-64a8c6ff3520)
- FDA Inspection 685831 - 2010-10-18
- FDA Inspection 560386 - 2009-02-04

Company: https://www.keypedia.com/companies/biopro-inc/4c9ccc95-f72f-4e0c-8479-e6d43484adb3

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