FDA Inspection
Hologic, IncHologic, Inc – FDA Inspection, Jun 29, 2017
Record Details
This FDA Inspection record concerns Hologic, Inc, with an inspection on June 29, 2017, issued by the New England District Office, covering medical devices & rad health.
- Company
- Hologic, Inc
- Inspection Date
- June 29, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 76a5925a-5774-4cab-b82c-0fa2bdcd2f7f
Inspection Facts
- Inspection number
- 1034462
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Hologic, Inc
6| Date | Classification | Office | Project area |
|---|---|---|---|
| November 4, 2025 | OAI | Compliance: Medical Devices | |
| September 24, 2024 | OAI | New England District Office | Compliance: Medical Devices |
| November 30, 2017 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| September 26, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 10, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Hologic, Inc
- FDA Inspection 1290240 - 2025-11-04
- FDA Inspection 1240946 - 2024-09-24
- FDA Inspection 1035885 - 2017-11-30
- FDA Inspection 850106 - 2013-09-26
- FDA Inspection 724038 - 2011-05-10
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