FDA Inspection 827823 — Hologic, Inc.

Hologic, Inc. — FEI 1221300

The FDA completed an inspection of Hologic, Inc. on April 15, 2013 in Bedford, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 15, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Bedford, MA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures