FDA Inspection 938784 — VBM Medizintechnik GmbH
The FDA completed an inspection of VBM Medizintechnik GmbH on July 24, 2015 in Sulz Am Neckar. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 24, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Sulz Am Neckar (Germany)