FDA inspection

ClearFlow Inc.: FDA inspection ending Oct 17, 2014

FDA inspection 901256 · No Action Indicated (NAI) · Irvine, CA

Key facts

Inspection ID 901256
Firm ClearFlow Inc.
FEI number 3008782989
Address 1630 S Sunkist St Ste E
City Irvine
State CA
ZIP 92618
Country United States
Fiscal year 2015
Inspection end date Oct 17, 2014
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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