# BioPro, Inc. – FDA Inspection, Nov 25, 2014

Source: https://www.keypedia.com/records/fda_inspections/biopro-inc/2cf225b3-11b0-48ec-ae1e-64a8c6ff3520
Source feed: FDA_Inspections

> FDA inspection 904881 of BioPro, Inc., November 25, 2014. Classification: Official Action Indicated (OAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 904881
- Company Name: BioPro, Inc.
- Inspection Date: 2014-11-25
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: 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 766155 - 2012-02-03](https://www.keypedia.com/records/fda_inspections/biopro-inc/82810946-20b2-4bbd-921f-f90c6c33f271)
- 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