FDA inspection
Antarma LLC: FDA inspection ending Jun 7, 2019
FDA inspection 1094963 · Voluntary Action Indicated (VAI) · New York, NY
Key facts
| Inspection ID | 1094963 |
|---|---|
| Firm | Antarma LLC |
| FEI number | 3014117096 |
| Address | 276 5th Ave Rm 704 |
| City | New York |
| State | NY |
| ZIP | 10001 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Jun 7, 2019 |
| 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