FDA Inspection 965150 — Acadia Pharmaceuticals Inc.

Acadia Pharmaceuticals Inc. — FEI 3005617555

The FDA completed an inspection of Acadia Pharmaceuticals Inc. on Feb 17, 2016 in San Diego, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 17, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
San Diego, CA (United States)

Additional Details

Sponsor, Contract Research Organization

Citations

IDCFRDescription
747921 CFR 312.56(a)Monitoring investigations
748221 CFR 312.50General responsibilities of sponsors

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