FDA Warning Letter — WHOOP, Inc.

Case 709755 — FEI 3031627845

The FDA took a Warning Letter action against WHOOP, Inc. on Jul 14, 2025 (Boston, MA). The action was issued by CDRH and concerns devices products.

Action details

Facility
WHOOP, Inc.
Date
Jul 14, 2025
Fiscal Year
2025
Product Type
Devices
Center
CDRH
Location
Boston, MA (United States)

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