FDA Inspection 839582 — MPS Anzon LLC
The FDA completed an inspection of MPS Anzon LLC on July 1, 2013 in Arcadia, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 1, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Arcadia, CA (United States)