FDA inspection
Trimedyne Inc: FDA inspection ending May 16, 2001
FDA inspection 75203 · No Action Indicated (NAI) · Corona, CA
Key facts
| Inspection ID | 75203 |
|---|---|
| Firm | Trimedyne Inc |
| FEI number | 1419951 |
| Address | 519 N Smith Ave Ste 105 |
| City | Corona |
| State | CA |
| ZIP | 92878-4315 |
| Fiscal year | 2001 |
| Inspection end date | May 16, 2001 |
| Classification | No Action Indicated (NAI) |
| 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
- None Citations
- None 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