FDA Inspection 1250877 — Bausch & Lomb Incorporated

Bausch & Lomb Incorporated — FEI 1032500

The FDA completed an inspection of Bausch & Lomb Incorporated on February 27, 2025 in Greenville, SC. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
February 27, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Greenville, SC (United States)

Citations

IDCFRDescription
121321 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
145121 CFR 211.113(b)Procedures for sterile drug products
361221 CFR 211.160(b)(3)Sampling/testing of drug products