FDA inspection

Carl Zeiss Meditec Production, LLC: FDA inspection ending May 10, 2016

FDA inspection 975176 · Voluntary Action Indicated (VAI) · Ontario, CA

Key facts

Inspection ID 975176
Firm Carl Zeiss Meditec Production, LLC
FEI number 3010126268
Address 1040 S Vintage Ave Ste A
City Ontario
State CA
ZIP 91761
Country United States
Fiscal year 2016
Inspection end date May 10, 2016
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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