# FDA Inspection 1043737 - Etiometry Inc. - February 16, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/etiometry-inc/b65dd9de-b039-4057-a639-575501d84422
Source feed: FDA_Inspections

> FDA Inspection 1043737 for Etiometry Inc. on February 16, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1043737
- Company Name: Etiometry Inc.
- Inspection Date: 2018-02-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/etiometry-inc/695e004c-4b9c-4ead-a617-617fdc5f4e78

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