Overview
- 6 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.
15 Aug 2014
21 CFR 211.22(d)
Procedures not in writing, fully followed
Cited by Katherine D Adams, Sharon K Thoma, Donna J Clevenger
15 Aug 2014
21 CFR 211.100(b)
Procedure Deviations Recorded and Justified
Cited by Katherine D Adams, Sharon K Thoma, Donna J Clevenger
15 Aug 2014
21 CFR 211.103
Actual vs. theoretical yields not determined
Cited by Katherine D Adams, Sharon K Thoma, Donna J Clevenger
15 Aug 2014
21 CFR 211.165(f)
Failing drug products not rejected
Cited by Katherine D Adams, Sharon K Thoma, Donna J Clevenger
15 Aug 2014
21 CFR 211.192
Investigations of discrepancies, failures
Cited by Katherine D Adams, Sharon K Thoma, Donna J Clevenger
Inspected site
MPMillennium Pharmaceuticals Inc.Cambridge, United States
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 211.100(b) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 211.103 | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 211.165(f) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 211.192 | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 211.22(d) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 314.81(b)(1)(ii) | Cited across public-safe Form 483 observations | 1x |
Full 483 report
Get the verbatim text of all 6 observations
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