FDA inspection

Spiracle Technology: FDA inspection ending Jun 18, 2013

FDA inspection 839854 · No Action Indicated (NAI) · Los Alamitos, CA

Key facts

Inspection ID 839854
Firm Spiracle Technology
FEI number 3000204983
Address 10601 Calle Lee Ste 190
City Los Alamitos
State CA
ZIP 90720
Country United States
Fiscal year 2013
Inspection end date Jun 18, 2013
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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