FDA Inspection 918047 — Erchonia Corporation, LLC

Erchonia Corporation, LLC — FEI 3003462036

The FDA completed an inspection of Erchonia Corporation, LLC on March 12, 2015 in Fountain Inn, SC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 12, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Fountain Inn, SC (United States)

Additional Details

Sponsor, Contract Research Organization