FDA Warning Letter — Neurolumen LLC
The FDA took a Warning Letter action against Neurolumen LLC on May 30, 2014 (Oklahoma City, OK). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.
Action Details
- Facility
- Neurolumen LLC
- Date
- May 30, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Center
- CDRH
- Location
- Oklahoma City, OK (United States)