FDA Inspection 1283358 — Multisource Manufacturing LLC

Multisource Manufacturing LLC — FEI 3010009632

The FDA completed an inspection of Multisource Manufacturing LLC on Sep 12, 2025 in Longmont, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 12, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Longmont, CO (United States)

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