# FDA Inspection 1047603 - RemetricHealth - March 06, 2018

Source: https://www.keypedia.com/records/fda_inspections/remetrichealth/6e50c08c-4ac2-4969-87d6-41e128977a7c
Source feed: FDA_Inspections

> FDA Inspection 1047603 for RemetricHealth on March 06, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1047603
- Company Name: RemetricHealth
- Inspection Date: 2018-03-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1225083 - 2023-11-15](https://www.keypedia.com/records/fda_inspections/remetrichealth/aece977d-d65f-49a3-a4b7-ddf1b0b2c994)

Company: https://www.keypedia.com/companies/remetrichealth/2689d33e-d5ab-46a9-8267-d2898bb81d4e

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