FDA Inspection 1035265 — Synchpack Inc.
The FDA completed an inspection of Synchpack Inc. on Dec 18, 2017 in Maple Grove, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 7 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Dec 18, 2017
- Fiscal Year
- 2018
- Product Type
- Food/Cosmetics
- Project Area
- Colors and Cosmetics Technology
- Location
- Maple Grove, MN (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15429 | 21 CFR 111.15(k) | Sanitation supervisors - assigned |
| 15532 | 21 CFR 111.255(b) | Batch record - complete |
| 15607 | 21 CFR 111.165(c)(2) | Product received - quality control; documentation; specs |
| 15645 | 21 CFR 111.455(c) | Hold - mix-up, contamination, deterioration |
| 15819 | 21 CFR 111.55 | Production, process controls - implement |
| 15897 | 21 CFR 111.83(a) | Reserve sample - collect, hold |
| 16004 | 21 CFR 111.130(b) | Quality control operations -returned dietary supplement; salvage, redistribution |