# Bausch & Lomb Inc – FDA Inspection, May 17, 2012

Source: https://www.keypedia.com/records/fda_inspections/bausch-lomb-inc/7bcf7ca4-5aab-4550-9359-5225a1103362
Source feed: FDA_Inspections

> FDA inspection 782300 of Bausch & Lomb Inc, May 17, 2012. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 806 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 782300
- Company Name: Bausch & Lomb Inc
- Inspection Date: 2012-05-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Documents

- FDA Inspection 1107226 - 2019-10-08
- [FDA Inspection 978030 - 2016-06-10](https://www.keypedia.com/records/fda_inspections/bausch-lomb-inc/e6b707f0-594e-4de6-88ca-206f4902697f)
- FDA Inspection 826558 - 2013-03-15
- FDA Inspection 784537 - 2012-06-01

Company: https://www.keypedia.com/companies/bausch-lomb-inc/6e2d24ec-25b4-419c-ba74-db88dd714834

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