FDA Inspection 1214579 — Mak-System Corp.

Mak-System Corp. — FEI 3000215342

The FDA completed an inspection of Mak-System Corp. on August 11, 2023 in Des Plaines, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 11, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Des Plaines, IL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation