Warning letter
Accelerated Analytical Laboratories Inc.: warning letter of Oct 18, 2017
FDA warning letter 534585 · Detroit District Office
Key facts
| Reference number | 534585 |
|---|---|
| Company | Accelerated Analytical Laboratories Inc. |
| Subject | CGMP/Finished Pharmaceuticals/Adulterated |
| Issue date | Oct 18, 2017 |
| Posted date | Oct 18, 2017 |
| Issuing office | Detroit District Office |
| Product type | Drugs |
| CFR sections cited | 210, 211.165(e) |
| Inspection city | Milwaukee |
| Inspection ZIP | 53224 |
| Inspection start date | May 8, 2017 |
| Letter on fda.gov | fda.gov |
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: