FDA Inspection 1192660 — ZYTO Technologies, Inc.

ZYTO Technologies, Inc. — FEI 3008493238

The FDA completed an inspection of ZYTO Technologies, Inc. on December 13, 2022 in Pleasant Grove, UT. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 7 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
December 13, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Pleasant Grove, UT (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
1472221 CFR 820.40Procedures not adequately established or maintained
232821 CFR 820.22Quality audits - auditor independence
310421 CFR 820.30(j)Design history file
337521 CFR 820.198(e)Records of complaint investigation
369621 CFR 820.100(b)Documentation
63121 CFR 803.17(a)(1)Lack of System for Event Evaluations