FDA Inspection 935262 — Avotec, Inc.

Avotec, Inc. — FEI 1000113348

The FDA completed an inspection of Avotec, Inc. on July 21, 2015 in Stuart, FL. 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
July 21, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Stuart, FL (United States)