FDA Inspection 1172024 — Maxkron Machine, LLC

Maxkron Machine, LLC — FEI 3018080016

The FDA completed an inspection of Maxkron Machine, LLC on May 13, 2022 in Valencia, CA. 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). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 13, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Valencia, CA (United States)