FDA Inspection 701114 — Hologic, Inc.

Hologic, Inc. — FEI 1220984

The FDA completed an inspection of Hologic, Inc. on Dec 15, 2010 in Danbury, CT. 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 15, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Danbury, CT (United States)

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