FDA inspection

American Medical Devices Inc: FDA inspection ending Oct 25, 2007

FDA inspection 494555 · No Action Indicated (NAI) · San Bernardino, CA

Key facts

Inspection ID 494555
Firm American Medical Devices Inc
FEI number 2024290
Address 287 S Stoddard Ave
City San Bernardino
State CA
ZIP 92401-2021
Fiscal year 2008
Inspection end date Oct 25, 2007
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

Browse all FDA inspections