FDA Inspection 746380 — Hologic, Inc.

Hologic, Inc. — FEI 1221300

The FDA completed an inspection of Hologic, Inc. on September 21, 2011 in Bedford, 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 21, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Bedford, MA (United States)