Overview
- 4 public-safe observations are available for this inspection.
- 1 structured CFR citation is represented.
- 1 investigator is tied to this Form 483.
Inspectional observations
Each observation cites the regulation FDA found the firm out of compliance with.
9 Mar 2016
21 CFR 111.210(d)
Master manufacturing record - ingredients list
Cited by Kimberly M Lichter
9 Mar 2016
21 CFR 111.210(d)
Master manufacturing record - Supplemental Facts
Cited by Kimberly M Lichter
9 Mar 2016
21 CFR 111.210(d)
Master manufacturing record - Supplemental Facts
Cited by Kimberly M Lichter
9 Mar 2016
21 CFR 111.210(d)
Master manufacturing record - ingredients list
Cited by Kimberly M Lichter
Inspected site
HMHerbalife Manufacturing, LLCLake Forest, United States
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 111.210(d) | Cited across public-safe Form 483 observations | 4x |
Full 483 report
Get the verbatim text of all 4 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