# FDA Inspection 782300 - Bausch & Lomb Inc - 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 for Bausch & Lomb Inc on May 17, 2012. Classification: Voluntary Action Indicated (VAI).

---

## Details

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

## Related Documents

- [FDA Inspection 1107226 - 2019-10-08](https://www.keypedia.com/records/fda_inspections/bausch-lomb-inc/c3b0a67a-3a59-44be-8e03-0ef2b47eaab0)
- [FDA Inspection 1107226 - 2019-10-08](https://www.keypedia.com/records/fda_inspections/bausch-lomb-inc/9386fbd5-d328-4230-aacc-8ce66162cbf8)
- [FDA Inspection 978030 - 2016-06-10](https://www.keypedia.com/records/fda_inspections/bausch-lomb-inc/5d56b0db-8ba2-4ba6-b971-b90f4de1324e)
- [FDA Inspection 978030 - 2016-06-10](https://www.keypedia.com/records/fda_inspections/bausch-lomb-inc/e6b707f0-594e-4de6-88ca-206f4902697f)
- [FDA Inspection 978030 - 2016-06-10](https://www.keypedia.com/records/fda_inspections/bausch-lomb-inc/42ebcf06-7707-48a0-9589-3ed17cb0f039)

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
