FDA inspection
NeoChild, LLC: FDA inspection ending Oct 30, 2015
FDA inspection 950996 · No Action Indicated (NAI) · Oklahoma City, OK
Key facts
| Inspection ID | 950996 |
|---|---|
| Firm | NeoChild, LLC |
| FEI number | 3006271008 |
| Address | 401 N Meridian Ave |
| City | Oklahoma City |
| State | OK |
| ZIP | 73107 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Oct 30, 2015 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data