# FDA Inspection 1052190 - Bodyline, Inc. - April 19, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/bodyline-inc/60672bde-e3ed-4c73-9e6b-9514da268741
Source feed: FDA_Inspections

> FDA Inspection 1052190 for Bodyline, Inc. on April 19, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1052190
- Company Name: Bodyline, Inc.
- Inspection Date: 2018-04-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1052190 - 2018-04-19](https://www.globalkeysolutions.net/records/fda_inspections/bodyline-inc/f8824375-6166-4556-b3dc-4738bd3be5b0)

Company: https://www.globalkeysolutions.net/companies/bodyline-inc/ec69ea1a-8825-4569-a31e-9ac9676cbf49

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