FDA inspection

Gliatech Inc: FDA inspection ending Nov 16, 2000

FDA inspection 53771 · Official Action Indicated (OAI) · Beachwood, OH

Key facts

Inspection ID 53771
Firm Gliatech Inc
FEI number 3001596592
Address 23420 Commerce Park
City Beachwood
State OH
ZIP 44122-5813
Fiscal year 2001
Inspection end date Nov 16, 2000
Classification Official Action Indicated (OAI)
Project area Product Evaluation: Med Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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