FDA Inspection 1224972 — NG Instruments, Inc.

NG Instruments, Inc. — FEI 3000205591

The FDA completed an inspection of NG Instruments, Inc. on Dec 14, 2023 in Warsaw, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 14, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Warsaw, IN (United States)

Citations

IDCFRDescription
312321 CFR 820.80(c)Lack of or inadequate In-process acceptance procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation