Warning letter
RAM Pharma, Inc: warning letter of Oct 27, 2017
FDA warning letter 526405 · Los Angeles District Office
Key facts
| Reference number | 526405 |
|---|---|
| Company | RAM Pharma, Inc |
| Subject | Compounding Pharmacy/Adulterated Drug Products |
| Issue date | Oct 27, 2017 |
| Posted date | Nov 21, 2017 |
| Issuing office | Los Angeles District Office |
| Product type | Drugs |
| CFR sections cited | 201.115, 210, 200.10(b), 211.28(a), 211.42(c)(10)(v), 211.42(c)(10)(vi), 211.113(b), 211.166(a), 211.167(a), 210.1(b) |
| Inspection city | Idaho Falls |
| Inspection ZIP | 83401 |
| Inspection start date | Feb 7, 2017 |
| Letter on fda.gov | fda.gov |
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: