# FDA Inspection 819785 - Bausch and Lomb, Incorporated - February 20, 2013

Source: https://www.keypedia.com/records/fda_inspections/bausch-and-lomb-incorporated/202f5d3f-96c6-48d3-9cbb-e439cb83dab3
Source feed: FDA_Inspections

> FDA Inspection 819785 for Bausch and Lomb, Incorporated on February 20, 2013. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 819785
- Company Name: Bausch and Lomb, Incorporated
- Inspection Date: 2013-02-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 811034 - 2012-12-13](https://www.keypedia.com/records/fda_inspections/bausch-and-lomb-incorporated/43cb6a64-ae43-42f9-9468-467ea793a40d)
- [FDA Inspection 811034 - 2012-12-13](https://www.keypedia.com/records/fda_inspections/bausch-and-lomb-incorporated/74317907-a3dc-4eb1-8d10-a5a692be0726)
- [FDA Inspection 606906 - 2009-08-19](https://www.keypedia.com/records/fda_inspections/bausch-and-lomb-incorporated/42f6c588-0a96-4f5c-b27b-9a58fd764d20)

Company: https://www.keypedia.com/companies/bausch-and-lomb-incorporated/55e74947-51ad-4df2-9776-d0f510e9b2c6

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