# FDA Inspection 1055321 - Metritrack Inc - May 03, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/metritrack-inc/f948d8ae-f775-46c7-88f9-d7dc5dc79f1b/
Source feed: FDA_Inspections

> FDA Inspection 1055321 for Metritrack Inc on May 03, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1055321
- Company Name: Metritrack Inc
- Inspection Date: 2018-05-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1261730 - 2025-02-11](https://www.globalkeysolutions.net/api/records/fda_inspections/metritrack-inc/983398dc-5517-4b40-b215-34c033bc878d/)
- [FDA Inspection 1055321 - 2018-05-03](https://www.globalkeysolutions.net/api/records/fda_inspections/metritrack-inc/3e8319ce-c2a2-48ec-8490-d81801ac6532/)

Company: https://www.globalkeysolutions.net/companies/metritrack-inc/2b05f6dc-8122-4be8-9e14-06df92c5a039

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