FDA inspection

Remel Inc.: FDA inspection ending Feb 3, 2025

FDA inspection 1259798 · Voluntary Action Indicated (VAI) · Oakwood Village, OH

Key facts

Inspection ID 1259798
Firm Remel Inc.
FEI number 1000515493
Address 1 Thermo Fisher Way
City Oakwood Village
State OH
ZIP 44146
Country United States
Fiscal year 2025
Inspection end date Feb 3, 2025
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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