FDA inspection
Camber Spine Technologies: FDA inspection ending Feb 13, 2019
FDA inspection 1084388 · No Action Indicated (NAI) · King Of Prussia, PA
Key facts
| Inspection ID | 1084388 |
|---|---|
| Firm | Camber Spine Technologies |
| FEI number | 3010197239 |
| Address | 501 Allendale Rd |
| City | King Of Prussia |
| State | PA |
| ZIP | 19406 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Feb 13, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Human Cellular, Tissue, and Gene Therapies |
| Product type | Biologics |
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