FDA Warning Letter — Klarity Medical Products LLC

Case 606982 — FEI 3001236129

The FDA took a Warning Letter action against Klarity Medical Products LLC on June 8, 2020 (Heath, OH). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Klarity Medical Products LLC
Date
June 8, 2020
Fiscal Year
2020
Product Type
Devices
Center
CDRH
Location
Heath, OH (United States)