FDA Inspection 850106 — Hologic, Inc

Hologic, Inc — FEI 1000120743

The FDA completed an inspection of Hologic, Inc on Sep 26, 2013 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
Sep 26, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Marlborough, MA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.