FDA Inspection 1228148 — WHPM Inc.
The FDA completed an inspection of WHPM Inc. on Jan 30, 2024 in Irwindale, CA. 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). 6 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jan 30, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Irwindale, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 14712 | 21 CFR 820.184 | DHR - not or inadequately maintained |
| 14720 | 21 CFR 820.50(a)(3) | Acceptable supplier records, inadequate records |
| 14721 | 21 CFR 820.70(g)(2) | Periodic equipment inspections |
| 3128 | 21 CFR 820.90(a) | Nonconforming product control |
| 3266 | 21 CFR 820.86 | Acceptance status |
| 3286 | 21 CFR 820.90(b)(1) | Procedures for product review,disposition lack of/inadequate |