FDA inspection
Nomax, Inc.: FDA inspection ending Oct 27, 2016
FDA inspection 991448 · Official Action Indicated (OAI) · Saint Louis, MO
Key facts
| Inspection ID | 991448 |
|---|---|
| Firm | Nomax, Inc. |
| FEI number | 1937310 |
| Address | 9735 Green Park Industrial Dr |
| City | Saint Louis |
| State | MO |
| ZIP | 63123 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Oct 27, 2016 |
| Classification | Official Action Indicated (OAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
| Warning letter | 512566 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes Warning letter followed
- Yes Form FDA 483 issued
- Yes Establishment inspection report (EIR) exists
- 10–99 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