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FDA inspection

Quest Diagnostics Nichols Institute: FDA inspection ending Apr 4, 2025

FDA inspection 1267374 · No Action Indicated (NAI) · San Juan Capistrano, California

Key facts

Inspection ID 1267374
Firm Quest Diagnostics Nichols Institute
FEI number 3007521501
Address 33608 Ortega Hwy
City San Juan Capistrano
State California
ZIP 92675
Fiscal year 2025
Inspection end date Apr 4, 2025
Classification No Action Indicated (NAI)
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

  • None Citations
  • None 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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