FDA Inspection 905500 — Multisource Manufacturing LLC

Multisource Manufacturing LLC — FEI 3010009632

The FDA completed an inspection of Multisource Manufacturing LLC on November 8, 2014 in Lafayette, CO. 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
November 8, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Lafayette, CO (United States)