FDA Inspection 1095941 — Modo, Inc.
The FDA completed an inspection of Modo, Inc. on Jun 7, 2019 in Tualatin, OR. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Jun 7, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Tualatin, OR (United States)