# FDA Inspection 590120 - Bausch & Lomb Inc - May 06, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/bausch-lomb-inc/f764a25f-4d48-4593-a2dd-d07e8fe655de/
Source feed: FDA_Inspections

> FDA Inspection 590120 for Bausch & Lomb Inc on May 06, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 590120
- Company Name: Bausch & Lomb Inc
- Inspection Date: 2009-05-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/bausch-lomb-inc/5d239f44-b435-487c-9b86-b5b406b65c68

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