FDA Inspection 1117803 — AcelRx Pharmaceuticals, Inc.

AcelRx Pharmaceuticals, Inc. — FEI 3006386491

The FDA completed an inspection of AcelRx Pharmaceuticals, Inc. on Feb 13, 2020 in Hayward, 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). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 13, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Hayward, CA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.