Warning letter
Arnold Tuber Industries Dba Sci-Dent, Inc [ARCHIVED]: warning letter of Nov 10, 2009
FDA warning letter 77085 · New York District Office
Key facts
| Reference number | 77085 |
|---|---|
| Company | Arnold Tuber Industries Dba Sci-Dent, Inc [ARCHIVED] |
| Subject | CGMP/QSR/Manufacture/Packing/Storage/Installation/Adulterated/Misbranded |
| Issue date | Nov 10, 2009 |
| Posted date | Nov 10, 2009 |
| Issuing office | New York District Office |
| Product type | Devices |
| CFR sections cited | 803, 803.17, 820, 807.81(b) |
| Inspection city | Orchard Park |
| Inspection ZIP | 14127 |
| Inspection start date | Jul 27, 2009 |
| 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: