FDA inspection

ARP Wave L.L.C.: FDA inspection ending Feb 7, 2017

FDA inspection 1002547 · Voluntary Action Indicated (VAI) · Apple Valley, MN

Key facts

Inspection ID 1002547
Firm ARP Wave L.L.C.
FEI number 3004509773
Address 7721 145th St W
City Apple Valley
State MN
ZIP 55124
Country United States
Fiscal year 2017
Inspection end date Feb 7, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 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

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