FDA inspection
Cutting Edge HC Brands: FDA inspection ending Jul 24, 2018
FDA inspection 1059873 · Voluntary Action Indicated (VAI) · Los Angeles, CA
Key facts
| Inspection ID | 1059873 |
|---|---|
| Firm | Cutting Edge HC Brands |
| FEI number | 3011285025 |
| Address | 314 N Alta Vista Blvd |
| City | Los Angeles |
| State | CA |
| ZIP | 90036 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Jul 24, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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