FDA inspection

Lincotek Medical LLC.: FDA inspection ending Nov 19, 2021

FDA inspection 1157207 · Voluntary Action Indicated (VAI) · Vandalia, OH

Key facts

Inspection ID 1157207
Firm Lincotek Medical LLC.
FEI number 3010039400
Address 811 Northwoods Blvd
City Vandalia
State OH
ZIP 45377
Country United States
Fiscal year 2022
Inspection end date Nov 19, 2021
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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