FDA Inspection 1196503 — MPS Anzon LLC

MPS Anzon LLC — FEI 3008182611

The FDA completed an inspection of MPS Anzon LLC on January 19, 2023 in Arcadia, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 19, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Arcadia, CA (United States)