FDA inspection

Device Masters Dental Laboratory L.L.C.: FDA inspection ending Nov 7, 2018

FDA inspection 1071078 · Voluntary Action Indicated (VAI) · Williamsburg, MI

Key facts

Inspection ID 1071078
Firm Device Masters Dental Laboratory L.L.C.
FEI number 3012702338
Address 6501 US Highway 31 N
City Williamsburg
State MI
ZIP 49690
Country United States
Fiscal year 2019
Inspection end date Nov 7, 2018
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 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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