FDA inspection
Sunrise Technologies Inc: FDA inspection ending Jun 1, 2000
FDA inspection 24841 · Voluntary Action Indicated (VAI) · Fremont, CA
Key facts
| Inspection ID | 24841 |
|---|---|
| Firm | Sunrise Technologies Inc |
| FEI number | 2939053 |
| Address | 3400 W Warren Ave |
| City | Fremont |
| State | CA |
| ZIP | 94538-6425 |
| Fiscal year | 2000 |
| Inspection end date | Jun 1, 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