FDA inspection

Lincotek Medical: FDA inspection ending Sep 21, 2023

FDA inspection 1219314 · No Action Indicated (NAI) · Bartlett, TN

Key facts

Inspection ID 1219314
Firm Lincotek Medical
FEI number 3008421730
Address 3110 Stage Post Dr Ste 101
City Bartlett
State TN
ZIP 38133
Country United States
Fiscal year 2023
Inspection end date Sep 21, 2023
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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