FDA Warning Letter — Multi-Med, Inc.
The FDA took a Warning Letter action against Multi-Med, Inc. on October 7, 2009 (Keene, NH). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- Multi-Med, Inc.
- Date
- October 7, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Center
- CDRH
- Location
- Keene, NH (United States)