FDA Inspection 944253 — Myriad Fiber Imaging Technologies, Inc.

Myriad Fiber Imaging Technologies, Inc. — FEI 3002516162

The FDA completed an inspection of Myriad Fiber Imaging Technologies, Inc. on September 18, 2015 in Dudley, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 6 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 18, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Dudley, MA (United States)

Citations

IDCFRDescription
312021 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
313021 CFR 820.100(a)Lack of or inadequate procedures
322621 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation