FDA Inspection 552241 — Medline Industries, LP
The FDA completed an inspection of Medline Industries, LP on Dec 11, 2008 in Northfield, IL. 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). 5 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Dec 11, 2008
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Northfield, IL (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3687 | 21 CFR 820.100(a)(1) | Analysis of data sources |
| 3689 | 21 CFR 820.100(a)(2) | Investigation |
| 479 | 21 CFR 820.50 | Purchasing controls, Lack of or inadequate procedures |
| 486 | 21 CFR 820.50(a) | Evaluation of suppliers, contractors, etc., requirements |
| 537 | 21 CFR 820.70(a) | Production processes |