FDA Inspection 833293 — Hologic, Inc.

Hologic, Inc. — FEI 2024800

The FDA completed an inspection of Hologic, Inc. on May 24, 2013 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). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 24, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Diego, CA (United States)

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