FDA inspection
Alma Lasers, Inc.: FDA inspection ending Jan 29, 2013
FDA inspection 816402 · Official Action Indicated (OAI) · Buffalo Grove, IL
Key facts
| Inspection ID | 816402 |
|---|---|
| Firm | Alma Lasers, Inc. |
| FEI number | 3004450661 |
| Address | 485 E Half Day Rd Ste 100 |
| City | Buffalo Grove |
| State | IL |
| ZIP | 60089 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Jan 29, 2013 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 394413 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes Warning letter followed
- Yes Form FDA 483 issued
- Yes 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