FDA Inspection 1052299 — Mindchild Medical, Inc.
The FDA completed an inspection of Mindchild Medical, Inc. on May 3, 2018 in North Andover, MA. 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
- May 3, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- North Andover, MA (United States)