FDA Inspection 919955 — Quest Diagnostics Nichols Institute

Quest Diagnostics Nichols Institute — FEI 3005010397

The FDA completed an inspection of Quest Diagnostics Nichols Institute on Mar 26, 2015 in Chantilly, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 26, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Chantilly, VA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.