FDA Inspection 790935 — Abbott Molecular, Inc.
The FDA completed an inspection of Abbott Molecular, Inc. on Jul 11, 2012 in Des Plaines, 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). 2 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jul 11, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Des Plaines, IL (United States)
Additional Details
Postmarket Audit Inspections
Citations
| ID | CFR | Description |
|---|---|---|
| 3128 | 21 CFR 820.90(a) | Nonconforming product control |
| 3696 | 21 CFR 820.100(b) | Documentation |