FDA inspection

Endotec, Inc.: FDA inspection ending May 20, 2004

FDA inspection 328389 · No Action Indicated (NAI) · Santa Fe Springs, CA

Key facts

Inspection ID 328389
Firm Endotec, Inc.
FEI number 3004553437
Address 14525 Valley View Ave Ste H
City Santa Fe Springs
State CA
ZIP 90670-5237
Fiscal year 2004
Inspection end date May 20, 2004
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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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