FDA Inspection 959872 — Anybattery, Inc.

Anybattery, Inc. — FEI 3005521864

The FDA completed an inspection of Anybattery, Inc. on December 16, 2015 in Rosemount, MN. 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
December 16, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Rosemount, MN (United States)