FDA inspection
Pretika Corporation: FDA inspection ending Oct 25, 2019
FDA inspection 1108019 · Voluntary Action Indicated (VAI) · Laguna Niguel, CA
Key facts
| Inspection ID | 1108019 |
|---|---|
| Firm | Pretika Corporation |
| FEI number | 3003493780 |
| Address | 28202 Cabot Rd Ste 300 |
| City | Laguna Niguel |
| State | CA |
| ZIP | 92677 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Oct 25, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 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