# FDA Inspection 1234273 - Distron Corporation - March 20, 2024

Source: https://www.keypedia.com/records/fda_inspections/distron-corporation/404441ab-5abd-4f86-b7e1-0b2c146812dd
Source feed: FDA_Inspections

> FDA Inspection 1234273 for Distron Corporation on March 20, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1234273
- Company Name: Distron Corporation
- Inspection Date: 2024-03-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1234273 - 2024-03-20](https://www.keypedia.com/records/fda_inspections/distron-corporation/7230f1e4-17e3-4265-9294-168d20ccd151)
- [FDA Inspection 1045305 - 2018-03-15](https://www.keypedia.com/records/fda_inspections/distron-corporation/0a618f13-7c1f-49e3-a260-a4bb0e4a108e)

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
