# FDA Inspection 1290240 - Hologic, Inc - November 04, 2025

Source: https://www.keypedia.com/records/fda_inspections/hologic-inc/4a8a2fb8-ac16-49c3-bc31-64dbff59b544
Source feed: FDA_Inspections

> FDA Inspection 1290240 for Hologic, Inc on November 04, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1290240
- Company Name: Hologic, Inc
- Inspection Date: 2025-11-04
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices

## Related Documents

- [FDA Inspection 1290240 - 2025-11-04](https://www.keypedia.com/records/fda_inspections/hologic-inc/997362c8-4c6a-4341-8243-0b5f5f1a1c91)
- [FDA Inspection 1290240 - 2025-11-04](https://www.keypedia.com/records/fda_inspections/hologic-inc/5c62a043-8e64-4289-8047-745d8519964a)
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- [FDA Inspection 1240946 - 2024-09-24](https://www.keypedia.com/records/fda_inspections/hologic-inc/16e62738-8902-400a-8522-363640a86504)
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Company: https://www.keypedia.com/companies/hologic-inc/4d48f318-a95f-441e-9118-6ce684212e08