# Bausch & Lomb Incorporated – FDA Inspection, Feb 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/805afebf-54f2-435f-afe6-2044741ba093
Source feed: FDA_Inspections

> FDA inspection 1001173 of Bausch & Lomb Incorporated, February 15, 2017. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1001173
- Company Name: Bausch & Lomb Incorporated
- Inspection Date: 2017-02-15
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 909049 - 2014-12-09
- FDA Inspection 667094 - 2010-06-09

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/matthew-d-schnittker/cf76f07f-db6d-47a0-8412-7eb084d4fe8b)

Company: https://www.keypedia.com/companies/bausch-lomb-incorporated/922a39c8-5fdc-4a83-81ca-b036bfd32784

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