FDA Inspection 1021891 — Aeroflot

Aeroflot — FEI 3012732301

The FDA completed an inspection of Aeroflot on Jun 28, 2017 in Dulles, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 28, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Technical Assistance: Food and Cosmetics
Location
Dulles, VA (United States)

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