FDA Inspection 977004 — Heron Therapeutics, Inc.

Heron Therapeutics, Inc. — FEI 3006138169

The FDA completed an inspection of Heron Therapeutics, Inc. on January 6, 2016 in Redwood City, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 6, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Redwood City, CA (United States)