FDA Inspection 785328 — Hologic, Inc.
The FDA completed an inspection of Hologic, Inc. on Jun 1, 2012 in Danbury, CT. 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
- Jun 1, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Danbury, CT (United States)