FDA inspection
Acro Biotech Inc.: FDA inspection ending May 1, 2018
FDA inspection 1050458 · Voluntary Action Indicated (VAI) · Rancho Cucamonga, CA
Key facts
| Inspection ID | 1050458 |
|---|---|
| Firm | Acro Biotech Inc. |
| FEI number | 3005670738 |
| Address | 9500 7th St Ste M |
| City | Rancho Cucamonga |
| State | CA |
| ZIP | 91730 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | May 1, 2018 |
| 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