FDA Warning Letter — 23andMe, Inc.
The FDA took a Warning Letter action against 23andMe, Inc. on November 22, 2013 (Mountain View, CA). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.
Action Details
- Facility
- 23andMe, Inc.
- Date
- November 22, 2013
- Fiscal Year
- 2014
- Product Type
- Devices
- Center
- CDRH
- Location
- Mountain View, CA (United States)