FDA inspection
ALOM Technologies Corporation: FDA inspection ending Oct 16, 2019
FDA inspection 1108200 · No Action Indicated (NAI) · Indianapolis, IN
Key facts
| Inspection ID | 1108200 |
|---|---|
| Firm | ALOM Technologies Corporation |
| FEI number | 3015489159 |
| Address | 3910 Waldemere Ave Unit 1 |
| City | Indianapolis |
| State | IN |
| ZIP | 46241 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Oct 16, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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