# FDA Inspection 857250 - Dilon Medical Technologies Inc. - November 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/dilon-medical-technologies-inc/ff2cbbab-df4a-4172-91d7-f724e533e66e
Source feed: FDA_Inspections

> FDA Inspection 857250 for Dilon Medical Technologies Inc. on November 19, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 857250
- Company Name: Dilon Medical Technologies Inc.
- Inspection Date: 2013-11-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/dilon-medical-technologies-inc/2e685c52-bcc7-43a2-8ff3-5d772af75e25

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