FDA inspection
DMX IMAGING, LLC: FDA inspection ending Apr 7, 2000
FDA inspection 19692 · Official Action Indicated (OAI) · Palm Harbor, FL
Key facts
| Inspection ID | 19692 |
|---|---|
| Firm | DMX IMAGING, LLC |
| FEI number | 1000221974 |
| Address | 4159 Corporate Ct Ste B |
| City | Palm Harbor |
| State | FL |
| ZIP | 34683-1480 |
| Fiscal year | 2000 |
| Inspection end date | Apr 7, 2000 |
| Classification | Official Action Indicated (OAI) |
| 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
- 1–9 Posted citations
- No 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