# FDA Inspection 800182 - FMS, Finapres Medical Systems BV - September 26, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/fms-finapres-medical-systems-bv/ffb53ed8-e4de-434b-a843-ac5a113a8645/
Source feed: FDA_Inspections

> FDA Inspection 800182 for FMS, Finapres Medical Systems BV on September 26, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 800182
- Company Name: FMS, Finapres Medical Systems BV
- Inspection Date: 2012-09-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 800182 - 2012-09-26](https://www.globalkeysolutions.net/api/records/fda_inspections/fms-finapres-medical-systems-bv/2448f46d-74e2-4633-9886-e99917d0c0f7/)

Company: https://www.globalkeysolutions.net/companies/fms-finapres-medical-systems-bv/4c6649fa-d7d1-4731-9e83-e9cc653d9a83

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