FDA inspection

ARP Wave L.L.C.: FDA inspection ending Oct 23, 2013

FDA inspection 852302 · No Action Indicated (NAI) · Apple Valley, MN

Key facts

Inspection ID 852302
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 2014
Inspection end date Oct 23, 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

Browse all FDA inspections