FDA inspection

MML Diagnostics Packaging, Inc: FDA inspection ending Jun 13, 2019

FDA inspection 1096454 · No Action Indicated (NAI) · Troutdale, OR

Key facts

Inspection ID 1096454
Firm MML Diagnostics Packaging, Inc
FEI number 3018348
Address 1625 Nw Sundial Rd
City Troutdale
State OR
ZIP 97060
Country United States
Fiscal year 2019
Inspection end date Jun 13, 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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