FDA inspection

Reflexonic, LLC: FDA inspection ending Apr 19, 2016

FDA inspection 968449 · Voluntary Action Indicated (VAI) · Mc Lean, VA

Key facts

Inspection ID 968449
Firm Reflexonic, LLC
FEI number 3009129589
Address 44055 Riverside Pkwy Ste 208
City Mc Lean
State VA
ZIP 22102
Country United States
Fiscal year 2016
Inspection end date Apr 19, 2016
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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