FDA Inspection 867315 — BioMarin Pharmaceutical Inc.

BioMarin Pharmaceutical Inc. — FEI 3010446870

The FDA completed an inspection of BioMarin Pharmaceutical Inc. on February 17, 2014 in San Rafael, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 17, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
San Rafael, CA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)