FDA Inspection 963398 — Antares Pharma, Inc.

Antares Pharma, Inc. — FEI 2182861

The FDA completed an inspection of Antares Pharma, Inc. on January 21, 2016 in Minnetonka, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 21, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Minnetonka, MN (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation
419121 CFR 806.10(a)(1)Report of risk to health