FDA Inspection 1007334 — Hologic, Inc.
The FDA completed an inspection of Hologic, Inc. on April 11, 2017 in Danbury, CT. 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
- April 11, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Danbury, CT (United States)
Additional Details
Postmarket Audit Inspections