Warning letter
Apheresis Technologies Inc.: warning letter of Nov 12, 1999
FDA warning letter UCM067856 · Florida District Office
Key facts
| Reference number | UCM067856 |
|---|---|
| Company | Apheresis Technologies Inc. |
| Subject | Quality System Regulation/Tubing Sets Plasma Filters and Blood Pumps |
| Issue date | Nov 12, 1999 |
| Posted date | Nov 12, 1999 |
| Issuing office | Florida District Office |
| Product type | Devices |
| CFR sections cited | 820 |
| Country | 3 |
| Inspection city | Palm Harbor |
| Inspection ZIP | 34683-5459 |
| Inspection start date | Oct 4, 1999 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- OAI Linked inspection classification
- Yes Form FDA 483 issued
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA warning letters
FDA warning letters notify a firm of significant regulatory violations found during an inspection or review and request prompt corrective action.
Source: U.S. Food and Drug Administration (FDA), Warning Letters · Source date: