FDA Inspection 1309198 — Global Products Group, LLC
The FDA completed an inspection of Global Products Group, LLC on March 25, 2026 in Bradenton, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 14 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- March 25, 2026
- Fiscal Year
- 2026
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Bradenton, FL (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15702 | 21 CFR 111.320(b) | Examination, testing; scientifically valid |
| 15723 | 21 CFR 111.365(i) | Metal, foreign material |
| 15858 | 21 CFR 111.75(a)(1)(i) | Component - verify identity, dietary ingredient |
| 15864 | 21 CFR 111.75(a)(2)(ii)(C) | Documentation - qualify supplier |
| 15953 | 21 CFR 111.113(a)(1) | Quality control production, process control; material review, disposition |
| 15995 | 21 CFR 111.127(d) | Quality control operations - packaged, labeled; specifications |
| 16001 | 21 CFR 111.130(a) | Quality control returned dietary supplement; material review, disposition |
| 22836 | 21 CFR 111.27(a) | Equipment - design - appropriate and suitable |
| 22840 | 21 CFR 111.35(b) | Make and keep records - equipment and utensils |
| 22843 | 21 CFR 111.70(b) | Specifications - components |
| 22847 | 21 CFR 111.70(e) | Specifications - finished dietary supplement |
| 22888 | 21 CFR 111.210 | Master manufacturing record - record requirements |
| 22890 | 21 CFR 111.260 | Batch record - required information |
| 22891 | 21 CFR 111.303 | Written procedures - establish; laboratory |