Warning letter
Maplerose Enterprises, LLC, dba Pencol Pharmacy: warning letter of Aug 2, 2017
FDA warning letter 520095 · Los Angeles District Office
Key facts
| Reference number | 520095 |
|---|---|
| Company | Maplerose Enterprises, LLC, dba Pencol Pharmacy |
| Subject | Compounding Pharmacy/Adulterated Drug Products |
| Issue date | Aug 2, 2017 |
| Posted date | Aug 15, 2017 |
| Issuing office | Los Angeles District Office |
| Product type | Drugs |
| CFR sections cited | 211.58, 200.10(b), 211.28(a), 211.42(c)(10)(v), 211.113(b), 211.167(a), 210.1(b) |
| Inspection city | Denver |
| Inspection ZIP | 80222 |
| Inspection start date | Aug 8, 2016 |
| 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: