FDA inspection
Red Oak Instruments, LLC: FDA inspection ending Nov 22, 2019
FDA inspection 1113768 · No Action Indicated (NAI) · Missouri City, TX
Key facts
| Inspection ID | 1113768 |
|---|---|
| Firm | Red Oak Instruments, LLC |
| FEI number | 3003786816 |
| Address | 21218 Kingsland Blvd |
| City | Missouri City |
| State | TX |
| ZIP | 77459 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Nov 22, 2019 |
| 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