FDA Inspection 786221 — Isto Biologics

Isto Biologics — FEI 3005610160

The FDA completed an inspection of Isto Biologics on Jun 15, 2012 in Saint Louis, MO. 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)
End Date
Jun 15, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)