FDA Inspection 1017731 — IodiTech, Inc.
The FDA completed an inspection of IodiTech, Inc. on July 13, 2017 in Kansas City, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 13, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Kansas City, MO (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3567 | 21 CFR 211.84(d)(2) | Component identification test |