FDA inspection

MML Diagnostics Packaging, Inc: FDA inspection ending Jul 6, 2012

FDA inspection 788947 · Voluntary Action Indicated (VAI) · Troutdale, OR

Key facts

Inspection ID 788947
Firm MML Diagnostics Packaging, Inc
FEI number 3018348
Address 1625 Nw Sundial Rd
City Troutdale
State OR
ZIP 97060
Country United States
Fiscal year 2012
Inspection end date Jul 6, 2012
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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