Warning letter
Aquarium Products: warning letter of May 3, 2006
FDA warning letter UCM075893 · Baltimore District Office
Key facts
| Reference number | UCM075893 |
|---|---|
| Company | Aquarium Products |
| Subject | CGMP Regulations for Finished Pharmaceuticals/Adulterated |
| Issue date | May 3, 2006 |
| Posted date | May 3, 2006 |
| Issuing office | Baltimore District Office |
| Product type | Drugs |
| CFR sections cited | 211, 211.22, 211.100, 211.166, 211.176, 211.67(b), 211.80(a), 211.101(a), 211.110(a), 211.165(a) |
| Country | 3 |
| Inspection city | Glen Burnie |
| Inspection ZIP | 21061 |
| Inspection start date | Jan 5, 2006 |
| Letter on fda.gov | web.archive.org |
At a glance
- 10–99 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: