FDA Inspection 998528 — Quest Diagnostics Nichols Institute

Quest Diagnostics Nichols Institute — FEI 3005010397

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

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