Warning letter
Enzyme Development Corporation: warning letter of Oct 25, 2001
FDA warning letter UCM178731 · Philadelphia District Office
Key facts
| Reference number | UCM178731 |
|---|---|
| Company | Enzyme Development Corporation |
| Subject | Active Pharmaceutical Ingredient Manufacturing Facility/Adulterated |
| Issue date | Oct 25, 2001 |
| Posted date | Oct 25, 2001 |
| Issuing office | Philadelphia District Office |
| Product type | Drugs |
| Country | 3 |
| Inspection city | Scranton |
| Inspection ZIP | 18504-2366 |
| Inspection start date | Jun 18, 2001 |
| Letter on fda.gov | web.archive.org |
At a glance
- 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: