FDA inspection

Neurolign USA, Llc: FDA inspection ending Oct 10, 2007

FDA inspection 491603 · Official Action Indicated (OAI) · Pittsburgh, PA

Key facts

Inspection ID 491603
Firm Neurolign USA, Llc
FEI number 2519945
Address 128 Gamma Dr
City Pittsburgh
State PA
ZIP 15238-2920
Fiscal year 2008
Inspection end date Oct 10, 2007
Classification Official Action Indicated (OAI)
Project area Compliance: Med 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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