FDA Warning Letter — 23andMe Genomics LLC

Case 415534 — FEI 3007699459

The FDA took a Warning Letter action against 23andMe Genomics LLC on November 22, 2013 (Palo Alto, CA). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
23andMe Genomics LLC
Date
November 22, 2013
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Palo Alto, CA (United States)