FDA Inspection 935262 — Avotec, Inc.

Avotec, Inc. — FEI 1000113348

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