FDA Inspection 1092849 — Capitol Vial

Capitol Vial — FEI 3000325731

The FDA completed an inspection of Capitol Vial on May 9, 2019 in Auburn, AL. 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
May 9, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Auburn, AL (United States)