FDA Inspection 792581 — SHENZHEN DELICA MEDICAL EQUIPMENT CO., LTD.
The FDA completed an inspection of SHENZHEN DELICA MEDICAL EQUIPMENT CO., LTD. on May 31, 2012 in Shenzhen. 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). 1 citation was issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- May 31, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Shenzhen (China)
Citations
| ID | CFR | Description |
|---|---|---|
| 3270 | 21 CFR 820.80(c) | Documentation |