FDA inspection
PureTek Corporation: FDA inspection ending Dec 15, 2017
FDA inspection 1034952 · Voluntary Action Indicated (VAI) · San Fernando, CA
Key facts
| Inspection ID | 1034952 |
|---|---|
| Firm | PureTek Corporation |
| FEI number | 1000125324 |
| Address | 1145 Arroyo St Ste D |
| City | San Fernando |
| State | CA |
| ZIP | 91340 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Dec 15, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No 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