FDA Inspection 950996 — NeoChild, LLC
The FDA completed an inspection of NeoChild, LLC on October 30, 2015 in Oklahoma City, OK. 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
- October 30, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Oklahoma City, OK (United States)