FDA Inspection 1053533 — Goldlife, LLC
The FDA completed an inspection of Goldlife, LLC on May 25, 2018 in Wilmington, DE. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 11 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- May 25, 2018
- Fiscal Year
- 2018
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Wilmington, DE (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15409 | 21 CFR 111.14(b)(1) | Personnel - records - written procedures |
| 15453 | 21 CFR 111.16 | Written procedures - cleaning |
| 15498 | 21 CFR 111.27(d) | Equipment - maintain, clean, sanitize |
| 15641 | 21 CFR 111.453 | Written procedures - holding |
| 15790 | 21 CFR 111.403 | Written procedures - labeling operations |
| 15791 | 21 CFR 111.403 | Written procedures -packaging operations |
| 15797 | 21 CFR 111.553 | Written procedures - product complaint |
| 15897 | 21 CFR 111.83(a) | Reserve sample - collect, hold |
| 15927 | 21 CFR 111.103 | Written procedures - quality control operations |
| 16040 | 21 CFR 111.610(a) | Records - available; FDA |
| 16042 | 21 CFR 111.503 | Written procedures - returned dietary supplement |