FDA Inspection 1079213 — Veranova LP

Veranova LP — FEI 2018076

The FDA completed an inspection of Veranova LP on January 31, 2019 in Devens, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 31, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Devens, MA (United States)