FDA inspection

Bausch & Lomb Incorporated: FDA inspection ending Feb 15, 2017

FDA inspection 1001173 · Voluntary Action Indicated (VAI) · Lancaster, NY

Key facts

Inspection ID 1001173
Firm Bausch & Lomb Incorporated
FEI number 1315522
Address 6 Lancaster Pkwy
City Lancaster
State NY
ZIP 14086
Country United States
Fiscal year 2017
Inspection end date Feb 15, 2017
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 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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