FDA Inspection
Hologic, Inc.Hologic, Inc. – FDA Inspection, Apr 15, 2013
Record Details
This FDA Inspection record concerns Hologic, Inc., with an inspection on April 15, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Hologic, Inc.
- Inspection Date
- April 15, 2013
- Product Type
- Devices
View Company Profile
ID · f4af53e7-7d13-4afc-998c-209d7fcf62b1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 827823
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Hologic, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 3, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 21, 2011 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| March 18, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Hologic, Inc.
- FDA Inspection 973191 - 2016-06-03
- FDA Inspection 746380 - 2011-09-21
- FDA Inspection 716947 - 2011-03-18
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