FDA inspection
Alma Lasers, Inc.: FDA inspection ending Nov 30, 2004
FDA inspection 357650 · Voluntary Action Indicated (VAI) · Buffalo Grove, IL
Key facts
| Inspection ID | 357650 |
|---|---|
| Firm | Alma Lasers, Inc. |
| FEI number | 3004450661 |
| Address | 485 E Half Day Rd Ste 100 |
| City | Buffalo Grove |
| State | IL |
| ZIP | 60089-8806 |
| Fiscal year | 2005 |
| Inspection end date | Nov 30, 2004 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| 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