FDA Inspection 1277076 — Myriad Fiber Imaging Technologies, Inc.

Myriad Fiber Imaging Technologies, Inc. — FEI 3002516162

The FDA completed an inspection of Myriad Fiber Imaging Technologies, Inc. on Jul 31, 2025 in Dudley, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 31, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Dudley, MA (United States)

Citations

IDCFRDescription
322621 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule
53721 CFR 820.70(a)Production processes

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