FDA inspection
Angiotech Biomaterials Corporation: FDA inspection ending Apr 30, 2001
FDA inspection 70753 · No Action Indicated (NAI) · Palo Alto, CA
Key facts
| Inspection ID | 70753 |
|---|---|
| Firm | Angiotech Biomaterials Corporation |
| FEI number | 3002203503 |
| Address | 2500 Faber Pl |
| City | Palo Alto |
| State | CA |
| ZIP | 94303-3329 |
| Fiscal year | 2001 |
| Inspection end date | Apr 30, 2001 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes 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