FDA Warning Letter — Lightwave
The FDA took a Warning Letter action against Lightwave on January 3, 2013 (Phoenix, AZ). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- Lightwave
- Date
- January 3, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Center
- CDRH
- Location
- Phoenix, AZ (United States)