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FDA Inspection 850106 — Hologic, Inc

Hologic, Inc — FEI 1000120743

The FDA completed an inspection of Hologic, Inc on September 26, 2013 in Marlborough, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 26, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Marlborough, MA (United States)

Facility

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Recent compliance actions

FDA data resources