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FDA Warning Letter — 23andMe Genomics LLC

Case 415534 — FEI 3007699459

The FDA took a Warning Letter action against 23andMe Genomics LLC on Nov 22, 2013 (Palo Alto, CA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

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

Facility

Recent inspections

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.