FDA Inspection 1040784 — MPS Anzon LLC
The FDA completed an inspection of MPS Anzon LLC on November 28, 2017 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
- November 28, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Arcadia, CA (United States)
Additional Details
Postmarket Audit Inspections