# FDA Inspection 1069353 - Depalt, Inc - August 02, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/depalt-inc/6f78ecd6-b704-46ff-af2a-4fec5a8f3f85
Source feed: FDA_Inspections

> FDA Inspection 1069353 for Depalt, Inc on August 02, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1069353
- Company Name: Depalt, Inc
- Inspection Date: 2018-08-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1069353 - 2018-08-02](https://www.globalkeysolutions.net/records/fda_inspections/depalt-inc/699f35eb-242d-4497-a660-1137dbab54ab)

Company: https://www.globalkeysolutions.net/companies/depalt-inc/62866e48-751f-43da-9445-0c61d7c10214

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