FDA inspection
Lumenis Inc.: FDA inspection ending Mar 8, 2000
FDA inspection 15833 · Voluntary Action Indicated (VAI) · San Jose, CA
Key facts
| Inspection ID | 15833 |
|---|---|
| Firm | Lumenis Inc. |
| FEI number | 2914019 |
| Address | 2077 Gateway Pl Ste 300 |
| City | San Jose |
| State | CA |
| ZIP | 95110-1149 |
| Fiscal year | 2000 |
| Inspection end date | Mar 8, 2000 |
| 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 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Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| Product type | Devices |
At a glance
- None 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