# Bausch & Lomb, Incorporated – FDA Inspection, Jul 13, 2018

Source: https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/7d228ae0-876d-4816-9904-3d209ef90540
Source feed: FDA_Inspections

> FDA inspection 1058969 of Bausch & Lomb, Incorporated, July 13, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1058969
- Company Name: Bausch & Lomb, Incorporated
- Inspection Date: 2018-07-13
- 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 893517 - 2014-08-13
- FDA Inspection 847745 - 2013-09-04
- FDA Inspection 682741 - 2010-09-28

## Related Officers

- [Tiki Dixon](https://www.keypedia.com/people/tiki-dixon/b3160a2c-ef16-4fa2-b9b9-4c3a0ed17c5b)

Company: https://www.keypedia.com/companies/bausch-lomb-incorporated/320f3528-910b-4bfa-a48f-11b1d4192d0e

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