FDA inspection

Greatbatch Ltd: FDA inspection ending Mar 28, 2006

FDA inspection 427746 · No Action Indicated (NAI) · Beaverton, OR

Key facts

Inspection ID 427746
Firm Greatbatch Ltd
FEI number 3002755179
Address 9305 SW Nimbus Ave
City Beaverton
State OR
ZIP 97008-7146
Fiscal year 2006
Inspection end date Mar 28, 2006
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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