# Bausch & Lomb Incorporated – FDA Inspection, Jul 31, 2013

Source: https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/2241014a-110c-45a1-9077-01bddc5ea0fc
Source feed: FDA_Inspections

> FDA inspection 843014 of Bausch & Lomb Incorporated, July 31, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 843014
- Company Name: Bausch & Lomb Incorporated
- Inspection Date: 2013-07-31
- 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: 2

## Related Documents

- [FDA Inspection 1157054 - 2018-08-09](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/4aa7ea27-0bb7-405d-b8be-70c92b0a5d05)
- FDA Inspection 720310 - 2011-04-18

Company: https://www.keypedia.com/companies/bausch-lomb-incorporated/8888b9c7-4ddb-41e5-97e2-63c3ac4578a3

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