# FDA Inspection 746412 - Numia Medical Technology, LLC - September 01, 2011

Source: https://www.keypedia.com/records/fda_inspections/numia-medical-technology-llc/01babe59-4fc6-4370-a7c9-e0880a950626
Source feed: FDA_Inspections

> FDA Inspection 746412 for Numia Medical Technology, LLC on September 01, 2011. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 746412
- Company Name: Numia Medical Technology, LLC
- Inspection Date: 2011-09-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 850575 - 2013-09-12](https://www.keypedia.com/records/fda_inspections/numia-medical-technology-llc/e1dbcf60-cae8-410e-961b-38ec19f6aa09)
- [FDA Inspection 850575 - 2013-09-12](https://www.keypedia.com/records/fda_inspections/numia-medical-technology-llc/bde2a5c0-b169-40cd-ad98-a097135a5b26)

Company: https://www.keypedia.com/companies/numia-medical-technology-llc/5b550384-d7fa-4c7f-9170-4653dcc31622

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7