FDA Inspection 1321542 — BioMarin Pharmaceutical, Inc.

BioMarin Pharmaceutical, Inc. — FEI 3004079983

The FDA completed an inspection of BioMarin Pharmaceutical, Inc. on Jun 9, 2026 in Novato, 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
Jun 9, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Novato, CA (United States)

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