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FDA inspection

Robling Medical LLC: FDA inspection ending Apr 6, 2026

FDA inspection 1311004 · Voluntary Action Indicated (VAI) · Youngsville, North Carolina

Key facts

Inspection ID 1311004
Firm Robling Medical LLC
FEI number 3007829657
Address 90 Weathers Ct
City Youngsville
State North Carolina
ZIP 27596
Fiscal year 2026
Inspection end date Apr 6, 2026
Classification Voluntary Action Indicated (VAI)
Project area Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Product Evaluation: Medical Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: Devices|Project Evaluation: 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
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

Other inspections at this establishment

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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