FDA Inspection 971963 — Reckitt Benckiser, LLC
The FDA completed an inspection of Reckitt Benckiser, LLC on May 12, 2016 in Mechanicsburg, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- May 12, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Mechanicsburg, PA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1560 | 21 CFR 110.35(c) | Lack of effective pest exclusion |
| 2327 | 21 CFR 820.22 | Quality audits - Lack of or inadequate procedures |
| 3696 | 21 CFR 820.100(b) | Documentation |
| 419 | 21 CFR 820.20(b) | Lack of or inadequate organizational structure |