FDA Inspection 1132715 — Keystone Heart Ltd

Keystone Heart Ltd — FEI 3012609179

The FDA completed an inspection of Keystone Heart Ltd on October 29, 2020 in Tampa, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 29, 2020
Fiscal Year
2021
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tampa, FL (United States)

Additional Details

Sponsor, Contract Research Organization

Citations

IDCFRDescription
292821 CFR 812.40Sponsors' general responsibilities