# FDA Inspection 1105935 - Primo Medical Group - October 03, 2019

Source: https://www.keypedia.com/records/fda_inspections/primo-medical-group/d2339e5a-9d54-4491-b89c-d3970d9eb7ac
Source feed: FDA_Inspections

> FDA Inspection 1105935 for Primo Medical Group on October 03, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1105935
- Company Name: Primo Medical Group
- Inspection Date: 2019-10-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1105935 - 2019-10-03](https://www.keypedia.com/records/fda_inspections/primo-medical-group/e41af818-8901-43b4-b729-6c6a0e1cd59a)
- [FDA Inspection 940287 - 2015-07-27](https://www.keypedia.com/records/fda_inspections/primo-medical-group/f098bf77-171a-4c63-bde6-8d4c6f5c0aa0)
- [FDA Inspection 711375 - 2011-02-18](https://www.keypedia.com/records/fda_inspections/primo-medical-group/0446c890-924e-4784-92a6-9ecf19c40521)
- [FDA Inspection 711375 - 2011-02-18](https://www.keypedia.com/records/fda_inspections/primo-medical-group/20aaeb00-0c60-43f0-ae05-973aa2a191e0)
- [FDA Inspection 627537 - 2009-11-06](https://www.keypedia.com/records/fda_inspections/primo-medical-group/3e788e5f-8321-4ec4-a473-9de6e25a97e0)

Company: https://www.keypedia.com/companies/primo-medical-group/557abba5-c59a-42a3-9bf1-5b8a0a3d287f

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