# FDA Inspection 835141 - Hologic, Inc. - May 24, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/hologic-inc/de3b3b03-3751-4cde-8a40-8b84b682e32f
Source feed: FDA_Inspections

> FDA Inspection 835141 for Hologic, Inc. on May 24, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 835141
- Company Name: Hologic, Inc.
- Inspection Date: 2013-05-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 835141 - 2013-05-24](https://www.globalkeysolutions.net/records/fda_inspections/hologic-inc/1c891b58-f3d2-4d8c-bc67-e569db7567d1)
- [FDA Inspection 698757 - 2010-11-17](https://www.globalkeysolutions.net/records/fda_inspections/hologic-inc/340bef81-63f2-4475-9b28-9bf35d760b45)
- [FDA Inspection 698757 - 2010-11-17](https://www.globalkeysolutions.net/records/fda_inspections/hologic-inc/938690d6-3af2-43c3-b7a3-1b7d4273a279)

Company: https://www.globalkeysolutions.net/companies/hologic-inc/f1027a99-79cc-42de-82f5-567b8e0cf4ed

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