FDA Inspection 579357 — Corin USA Limited

Corin USA Limited — FEI 1000131827

The FDA completed an inspection of Corin USA Limited on Apr 28, 2009 in Tampa, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 28, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tampa, FL (United States)

Additional Details

Sponsor, Contract Research Organization