# FDA Inspection 672417 - Hologic, Inc. - July 15, 2010

Source: https://www.keypedia.com/records/fda_inspections/hologic-inc/b8939e05-29d3-47cb-be62-a858a6b367eb
Source feed: FDA_Inspections

> FDA Inspection 672417 for Hologic, Inc. on July 15, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 672417
- Company Name: Hologic, Inc.
- Inspection Date: 2010-07-15
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 854451 - 2013-09-18](https://www.keypedia.com/records/fda_inspections/hologic-inc/d4a95b03-dc53-43dc-95af-8107d1694279)
- [FDA Inspection 672417 - 2010-07-15](https://www.keypedia.com/records/fda_inspections/hologic-inc/ad4d0c76-f23d-4fe9-bda7-b952bcdc31ce)
- [FDA Inspection 560774 - 2009-02-05](https://www.keypedia.com/records/fda_inspections/hologic-inc/e340b251-971a-4544-9138-4512c7b48747)

Company: https://www.keypedia.com/companies/hologic-inc/a6cce412-c309-4422-a14f-25cda7885406

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7