FDA Warning Letter — ReNovo, Inc.

Case 664014 — FEI 3014023545

The FDA took a Warning Letter action against ReNovo, Inc. on October 13, 2023 (Bend, OR). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
ReNovo, Inc.
Date
October 13, 2023
Fiscal Year
2024
Product Type
Devices
Center
CDRH
Location
Bend, OR (United States)