FDA Inspection 1267209 — RevZero, Inc.

RevZero, Inc. — FEI 3010068573

The FDA completed an inspection of RevZero, Inc. on April 18, 2025 in Chanhassen, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 18, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chanhassen, MN (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures