# FDA Inspection 878932 - Thompson MIS - May 08, 2014

Source: https://www.keypedia.com/records/fda_inspections/thompson-mis/ecef065b-bcb6-4491-8d7a-68163eda2e92
Source feed: FDA_Inspections

> FDA Inspection 878932 for Thompson MIS on May 08, 2014. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 878932
- Company Name: Thompson MIS
- Inspection Date: 2014-05-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 988819 - 2016-10-11](https://www.keypedia.com/records/fda_inspections/thompson-mis/d0f14e2f-14c8-4be3-bc95-66b5c0009cbf)
- [FDA Inspection 779815 - 2012-05-02](https://www.keypedia.com/records/fda_inspections/thompson-mis/babd6113-7d31-4918-a478-7b543f4a478c)

Company: https://www.keypedia.com/companies/thompson-mis/26c35186-75da-4786-a4c0-b8b9dc3b91ed

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