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FDA Inspection 1270643 — Quest Diagnostics Nichols Institute

Quest Diagnostics Nichols Institute — FEI 3005010397

The FDA completed an inspection of Quest Diagnostics Nichols Institute on May 15, 2025 in Chantilly, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 15, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Chantilly, VA (United States)

Facility

Other inspections at this facility

  • 1150115 (NAI Mon Aug 30 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1102830 (VAI Mon Sep 23 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 998528 (NAI Thu Jan 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 919955 (NAI Thu Mar 26 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 835530 (VAI Wed Jun 19 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources