# FDA Inspection 1029220 - Diatron US Inc. - September 06, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/diatron-us-inc/df726a30-3085-4fdb-9ba9-bcfe4a5c3b75
Source feed: FDA_Inspections

> FDA Inspection 1029220 for Diatron US Inc. on September 06, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029220
- Company Name: Diatron US Inc.
- Inspection Date: 2017-09-06
- 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 1029220 - 2017-09-06](https://www.globalkeysolutions.net/records/fda_inspections/diatron-us-inc/9bbabf7c-1ad4-4c7b-bdf2-93368a89a6ad)

Company: https://www.globalkeysolutions.net/companies/diatron-us-inc/56ef2191-2a94-4bbb-8cea-5b46b583cbf8

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