# Bausch & Lomb Incorporated - Inspection Records

Source: https://www.keypedia.com/companies/bausch-lomb-incorporated/989fe252-9728-4751-92ab-c4b18fa5eff8

> Inspection records and compliance data for Bausch & Lomb Incorporated in Greenville, South Carolina. Access full analysis and detailed observations.

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## Details

- Name: Bausch & Lomb Incorporated
- FEI Number: 1032500
- City: Greenville
- State: South Carolina
- Country Name: United States
- Address Line 1: 8507 Pelham Rd
- Zip Code: 29615
- Facility Type: Medical Device/Pharmaceutical Manufacturer

## Related Documents

- [483 - Bausch & Lomb Incorporated - 2025-02-27](https://www.keypedia.com/records/483/bausch-lomb-incorporated/01c8a6ee-84d6-4898-9b59-37e38def9333) — source: FDA, date: February 27, 2025
- [FDA Inspection 1250877 - Bausch & Lomb Incorporated - 2025-02-27](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/fdade0a7-d53d-4168-a118-6b9dac94a928) — classification: Official Action Indicated (OAI), source: FDA, date: February 27, 2025
- [FDA Inspection 1073462 - Bausch & Lomb Incorporated - 2018-08-28](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/e9c423e8-1855-4f4d-aced-0bd2ba45075e) — classification: No Action Indicated (NAI), source: FDA, date: August 28, 2018
- [FDA Inspection 1073462 - Bausch & Lomb Incorporated - 2018-08-28](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/3dff6074-7967-4758-b28f-07dcb8744e73) — classification: No Action Indicated (NAI), source: FDA, date: August 28, 2018
- [FDA Inspection 1031429 - Bausch & Lomb Incorporated - 2017-09-15](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/6cbfe870-9327-413c-abe5-70837dd9eaae) — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2017
- [FDA Inspection 988726 - Bausch & Lomb Incorporated - 2016-10-05](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/458ffa93-54c8-4333-ad1c-9fed1e14db84) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 5, 2016
- [FDA Inspection 988726 - Bausch & Lomb Incorporated - 2016-10-05](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/c8c23e8a-463b-4e3c-9b8d-ecc5be07c778) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 5, 2016
- [FDA Inspection 911396 - Bausch & Lomb Incorporated - 2015-01-15](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/fe527c79-a13b-48d8-a70e-634bf5064ae9) — classification: No Action Indicated (NAI), source: FDA, date: January 15, 2015
- [FDA Inspection 911396 - Bausch & Lomb Incorporated - 2015-01-15](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/c0a331dc-70d7-4813-85fa-a5697b6b5cde) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 15, 2015
- [FDA Inspection 820858 - Bausch & Lomb Incorporated - 2013-02-08](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/8133e795-486c-4e28-89a6-3e753573a104) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 8, 2013
- [FDA Inspection 820858 - Bausch & Lomb Incorporated - 2013-02-08](https://www.keypedia.com/records/fda_inspections/bausch-lomb-incorporated/b8057638-dbec-404a-8cc1-fc05dd3642f2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 8, 2013
- [483 - Bausch & Lomb Incorporated - 2006-05-15](https://www.keypedia.com/records/483/bausch-lomb-incorporated/7d50142b-ed55-41e3-b196-18edb1340d4e) — source: FDA, date: May 15, 2006

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