FDA inspection
Pelvalon, Inc.: FDA inspection ending Aug 28, 2019
FDA inspection 1102422 · No Action Indicated (NAI) · San Francisco, CA
Key facts
| Inspection ID | 1102422 |
|---|---|
| Firm | Pelvalon, Inc. |
| FEI number | 3009131020 |
| Address | 2880 Lakeside Dr Ste 201 |
| City | San Francisco |
| State | CA |
| ZIP | 94127 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Aug 28, 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