FDA inspection

Surgik LC: FDA inspection ending Sep 16, 2016

FDA inspection 986018 · Voluntary Action Indicated (VAI) · Tulsa, OK

Key facts

Inspection ID 986018
Firm Surgik LC
FEI number 3006408264
Address 11672 E 51st St
City Tulsa
State OK
ZIP 74146
Country United States
Fiscal year 2016
Inspection end date Sep 16, 2016
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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