FDA inspection

SureTek Medical: FDA inspection ending Jul 25, 2012

FDA inspection 797481 · Voluntary Action Indicated (VAI) · Greenville, SC

Key facts

Inspection ID 797481
Firm SureTek Medical
FEI number 3005575604
Address 25B Maple Creek Cir
City Greenville
State SC
ZIP 29607
Country United States
Fiscal year 2012
Inspection end date Jul 25, 2012
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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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