FDA Warning Letter — American Ultraviolet Co.
The FDA took a Warning Letter action against American Ultraviolet Co. on Jun 4, 2009 (Lebanon, IN). The action was issued by CDRH and concerns devices products.
Action Details
- Facility
- American Ultraviolet Co.
- Date
- Jun 4, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Center
- CDRH
- Location
- Lebanon, IN (United States)