FDA inspection

Spiracle Technology: FDA inspection ending Aug 7, 2019

FDA inspection 1101567 · No Action Indicated (NAI) · Los Alamitos, CA

Key facts

Inspection ID 1101567
Firm Spiracle Technology
FEI number 3000204983
Address 10601 Calle Lee Ste 190
City Los Alamitos
State CA
ZIP 90720-6788
Fiscal year 2019
Inspection end date Aug 7, 2019
Classification No Action Indicated (NAI)
Project area Compliance: Medical 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