FDA Inspection 1016391 — MV Transatlantic

MV Transatlantic — FEI 3013506274

The FDA completed an inspection of MV Transatlantic on May 16, 2017 in Greenwich, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 16, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Technical Assistance: Food and Cosmetics
Location
Greenwich, CT (United States)

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