Bausch & Lomb Incorporated

Form 483

Greenville, South Carolina, United StatesFEI 1032500Issued May 12, 2009

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1032500.

Observations10

Issue DateMay 12, 2009

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Bausch & Lomb Incorporated
Location: Greenville, South Carolina, United States
FEI Number: 1032500
Product Type: Devices
Issue Date: May 12, 2009
Country: United States

Inspection History, 2009 to 2025

NAI4

VAI5

OAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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Bausch & Lomb Incorporated FDA Form 483, Greenville, South Carolina, May 12, 2009