FDA Inspection 640101 — Heron Therapeutics, Inc.

Heron Therapeutics, Inc. — FEI 3006138169

The FDA completed an inspection of Heron Therapeutics, Inc. on January 21, 2010 in Redwood City, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
January 21, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Redwood City, CA (United States)