FDA Warning Letter — Klarity Medical Products LLC

Case 606982 — FEI 3001236129

The FDA took a Warning Letter action against Klarity Medical Products LLC on Jun 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
Jun 8, 2020
Fiscal Year
2020
Product Type
Devices
Center
CDRH
Location
Heath, OH (United States)

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