FDA Warning Letter — Conformis Inc.

Case 596362 — FEI 3004153240

The FDA took a Warning Letter action against Conformis Inc. on December 10, 2019 (Wilmington, MA). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Conformis Inc.
Date
December 10, 2019
Fiscal Year
2020
Product Type
Devices
Center
CDRH
Location
Wilmington, MA (United States)