# FDA Inspection 1045305 - Distron Corporation - March 15, 2018

Source: https://www.keypedia.com/records/fda_inspections/distron-corporation/0a618f13-7c1f-49e3-a260-a4bb0e4a108e
Source feed: FDA_Inspections

> FDA Inspection 1045305 for Distron Corporation on March 15, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1045305
- Company Name: Distron Corporation
- Inspection Date: 2018-03-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/distron-corporation/d8c4d6b5-a633-4c6e-99db-4b4cbd090be9

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