FDA inspection

Solo-Dex, Inc.: FDA inspection ending Nov 14, 2019

FDA inspection 1110661 · No Action Indicated (NAI) · Wolf Creek, MT

Key facts

Inspection ID 1110661
Firm Solo-Dex, Inc.
FEI number 3010592727
Address 2840 Wilderness Pl Ste D
City Wolf Creek
State MT
ZIP 59648
Country United States
Fiscal year 2020
Inspection end date Nov 14, 2019
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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