FDA Inspection 1294380 — MFG One, LLC

MFG One, LLC — FEI 3004167615

The FDA completed an inspection of MFG One, LLC on Dec 2, 2025 in Chantilly, VA. 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
Dec 2, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chantilly, VA (United States)

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