FDA Inspection 1089207 — Novosource, LLC

Novosource, LLC — FEI 3014273644

The FDA completed an inspection of Novosource, LLC on March 20, 2019 in Morgantown, WV. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 20, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Morgantown, WV (United States)