Overview
- 12 public-safe observations are available for this inspection.
- 6 structured CFR citations are represented.
- 3 investigators are tied to this Form 483.
Inspectional observations
Each observation cites the regulation FDA found the firm out of compliance with.
11 Apr 2019
21 CFR 211.198(a)
Quality Control Review
Cited by Jennifer Lalama, Jose E Melendez, Adaliz Santaliz-Cruz
11 Apr 2019
21 CFR 211.198(a)
Quality Control Review
Cited by Jennifer Lalama, Jose E Melendez, Adaliz Santaliz-Cruz
11 Apr 2019
21 CFR 211.22(d)
Procedures not in writing, fully followed
Cited by Jennifer Lalama, Jose E Melendez, Adaliz Santaliz-Cruz
11 Apr 2019
21 CFR 211.22(d)
Procedures not in writing, fully followed
Cited by Jennifer Lalama, Jose E Melendez, Adaliz Santaliz-Cruz
11 Apr 2019
21 CFR 606.171
Biological product deviation report
Cited by Jennifer Lalama, Jose E Melendez, Adaliz Santaliz-Cruz
Inspected site
AMAmgen Manufacturing Limited LLCJuncos, United States
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 211.198(a) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 211.22(d) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 606.171 | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 820.100(a) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 820.30(f) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 820.50 | Cited across public-safe Form 483 observations | 2x |
Source document
PDF
PDF available
Form 483 source document
The source document is available to authorized Atlas users.
Full 483 report
Get the verbatim text of all 12 observations
The source PDF and every observation in full, so your team sees exactly what was cited and how it was answered.
- The site's full inspection history around this Form 483
- Whether these citations escalated to a warning letter
- The investigators involved and the citations they repeat elsewhere