FDA Inspection 682741 — Bausch & Lomb, Incorporated

Bausch & Lomb, Incorporated — FEI 1000305478

The FDA completed an inspection of Bausch & Lomb, Incorporated on Sep 28, 2010 in Lynchburg, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 28, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lynchburg, VA (United States)

Citations

IDCFRDescription
328621 CFR 820.90(b)(1)Procedures for product review,disposition lack of/inadequate
366921 CFR 820.20(c)Management review - defined interval, sufficient frequency
369621 CFR 820.100(b)Documentation