# FDA Inspection 969090 - Norvich - March 04, 2016

Source: https://www.keypedia.com/records/fda_inspections/norvich/02b4878f-7c5f-49bc-9362-9dd6abd2614c
Source feed: FDA_Inspections

> FDA Inspection 969090 for Norvich on March 04, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 969090
- Company Name: Norvich
- Inspection Date: 2016-03-04
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/norvich/b1c49f52-ee50-4d5b-beac-13d2f627cc7b

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