FDA Inspection 823976 — Digicare Biomedical Technology, Inc.
The FDA completed an inspection of Digicare Biomedical Technology, Inc. on Mar 12, 2013 in Boynton Beach, FL. 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
- Mar 12, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Boynton Beach, FL (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 2371 | 21 CFR 820.30(a) | Design control - no procedures |
| 479 | 21 CFR 820.50 | Purchasing controls, Lack of or inadequate procedures |