FDA Inspection
Freeman Enterprise LLCFreeman Enterprise LLC – FDA Inspection, Dec 16, 2014
Record Details
This FDA Inspection record concerns Freeman Enterprise LLC, with an inspection on December 16, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Freeman Enterprise LLC
- Inspection Date
- December 16, 2014
- Product Type
- Devices
View Company Profile
ID · 47371d5e-1424-4280-b487-f20ebe1cd7e4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 907129
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Freeman Enterprise LLC
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 7, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 29, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 23, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 4, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Freeman Enterprise LLC
- FDA Inspection 1081836 - 2019-03-07
- FDA Inspection 716628 - 2011-03-29
- FDA Inspection 668234 - 2010-06-23
- FDA Inspection 611065 - 2009-09-04
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.