FDA inspection

Orthomed Llc: FDA inspection ending Sep 13, 2016

FDA inspection 989467 · No Action Indicated (NAI) · Whittier, CA

Key facts

Inspection ID 989467
Firm Orthomed Llc
FEI number 3009142693
Address 9834 Norwalk Blvd
City Whittier
State CA
ZIP 90605
Country United States
Fiscal year 2016
Inspection end date Sep 13, 2016
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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