# FDA Inspection 704851 - Bausch & Lomb Incorporated - December 17, 2010

Source: https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/5fad4d30-c8b9-4744-b5f7-dde48ebcab68
Source feed: FDA_Inspections

> FDA Inspection 704851 for Bausch & Lomb Incorporated on December 17, 2010. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 704851
- Company Name: Bausch & Lomb Incorporated
- Inspection Date: 2010-12-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1250877 - 2025-02-27](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/fdade0a7-d53d-4168-a118-6b9dac94a928)
- [FDA Inspection 1073462 - 2018-08-28](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/e9c423e8-1855-4f4d-aced-0bd2ba45075e)
- [FDA Inspection 1073462 - 2018-08-28](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/3dff6074-7967-4758-b28f-07dcb8744e73)
- [FDA Inspection 1031429 - 2017-09-15](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/6cbfe870-9327-413c-abe5-70837dd9eaae)
- [FDA Inspection 988726 - 2016-10-05](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/458ffa93-54c8-4333-ad1c-9fed1e14db84)

Company: https://www.keypedia.com/companies/bausch-lomb-incorporated/989fe252-9728-4751-92ab-c4b18fa5eff8

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