FDA Inspection
BioPro, Inc.BioPro, Inc. – FDA Inspection, Nov 25, 2014
Record Details
This FDA Inspection record concerns BioPro, Inc., with an inspection on November 25, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- BioPro, Inc.
- Inspection Date
- November 25, 2014
- Product Type
- Devices
View Company Profile
ID · 2cf225b3-11b0-48ec-ae1e-64a8c6ff3520
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 904881
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of BioPro, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 7, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 3, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 18, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 4, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for BioPro, Inc.
- FDA Inspection 947607 - 2015-10-07
- FDA Inspection 766155 - 2012-02-03
- FDA Inspection 685831 - 2010-10-18
- FDA Inspection 560386 - 2009-02-04
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.