FDA Inspection 1035885 — Hologic, Inc

Hologic, Inc — FEI 1000120743

The FDA completed an inspection of Hologic, Inc on Nov 30, 2017 in Marlborough, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 30, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Marlborough, MA (United States)

Additional Details

Sponsor, Contract Research Organization

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