FDA inspection

Endotec, Inc.: FDA inspection ending Oct 14, 2016

FDA inspection 991826 · Voluntary Action Indicated (VAI) · Santa Fe Springs, CA

Key facts

Inspection ID 991826
Firm Endotec, Inc.
FEI number 3004553437
Address 14525 Valley View Ave Ste H
City Santa Fe Springs
State CA
ZIP 90670
Country United States
Fiscal year 2017
Inspection end date Oct 14, 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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