FDA inspection

Bausch & Lomb Incorporated: FDA inspection ending Mar 12, 2015

FDA inspection 921919 · No Action Indicated (NAI) · Irvine, CA

Key facts

Inspection ID 921919
Firm Bausch & Lomb Incorporated
FEI number 3003434767
Address 15273 Alton Pkwy Ste 200
City Irvine
State CA
ZIP 92618
Country United States
Fiscal year 2015
Inspection end date Mar 12, 2015
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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