FDA inspection

MML Diagnostics Packaging, Inc: FDA inspection ending Nov 12, 2003

FDA inspection 301111 · No Action Indicated (NAI) · Troutdale, OR

Key facts

Inspection ID 301111
Firm MML Diagnostics Packaging, Inc
FEI number 3018348
Address 1625 Nw Sundial Rd
City Troutdale
State OR
ZIP 97060-9553
Fiscal year 2004
Inspection end date Nov 12, 2003
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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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