FDA Inspection 1073695 — Antares Pharma, Inc.

Antares Pharma, Inc. — FEI 2182861

The FDA completed an inspection of Antares Pharma, Inc. on December 4, 2018 in Minnetonka, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 4, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Minnetonka, MN (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation