FDA inspection

Danmar Products, Inc.: FDA inspection ending Apr 12, 2010

FDA inspection 658929 · Voluntary Action Indicated (VAI) · Ann Arbor, MI

Key facts

Inspection ID 658929
Firm Danmar Products, Inc.
FEI number 1831680
Address 221 Jackson Industrial Dr
City Ann Arbor
State MI
ZIP 48103
Country United States
Fiscal year 2010
Inspection end date Apr 12, 2010
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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