# FDA Inspection 1043830 - Dilon Technologies Inc - February 26, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/dilon-technologies-inc/a0834c44-9118-4574-a64d-73512b49c231
Source feed: FDA_Inspections

> FDA Inspection 1043830 for Dilon Technologies Inc on February 26, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1043830
- Company Name: Dilon Technologies Inc
- Inspection Date: 2018-02-26
- 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 1043830 - 2018-02-26](https://www.globalkeysolutions.net/records/fda_inspections/dilon-technologies-inc/f8dce374-46a2-4805-b4f6-1c6b2641bf1f)

Company: https://www.globalkeysolutions.net/companies/dilon-technologies-inc/efcddd7a-8f8e-4b6a-9350-762446ac872e

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