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FDA inspection

Cousin Biotech SAS: FDA inspection ending Apr 3, 2025

FDA inspection 1267763 · Voluntary Action Indicated (VAI) · Wervicq-Sud

Key facts

Inspection ID 1267763
Firm Cousin Biotech SAS
FEI number 3003258310
Address Allee Des Roses
City Wervicq-Sud
Fiscal year 2025
Inspection end date Apr 3, 2025
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical 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.

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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