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FDA Inspection 998528 — Quest Diagnostics Nichols Institute

Quest Diagnostics Nichols Institute — FEI 3005010397

The FDA completed an inspection of Quest Diagnostics Nichols Institute on January 12, 2017 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
January 12, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Chantilly, VA (United States)

Facility

Other inspections at this facility

  • 1270643 (NAI Thu May 15 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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))
  • 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