FDA Inspection 1119699 — Murata Vios, Inc.
The FDA completed an inspection of Murata Vios, Inc. on February 20, 2020 in Woodbury, MN. 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
- February 20, 2020
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Woodbury, MN (United States)