# FDA Inspection 1026753 - Ludwig Medical, Inc - September 26, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/ludwig-medical-inc/ba9138e4-fccb-4d98-92fd-17ef160b07b8
Source feed: FDA_Inspections

> FDA Inspection 1026753 for Ludwig Medical, Inc on September 26, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026753
- Company Name: Ludwig Medical, Inc
- Inspection Date: 2017-09-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1026753 - 2017-09-26](https://www.globalkeysolutions.net/records/fda_inspections/ludwig-medical-inc/cbb10957-0a57-43fa-825e-677633a5f37d)
- [FDA Inspection 780305 - 2012-05-07](https://www.globalkeysolutions.net/records/fda_inspections/ludwig-medical-inc/8d10f47b-5623-40ba-8bfb-37e1ab89c296)
- [FDA Inspection 780305 - 2012-05-07](https://www.globalkeysolutions.net/records/fda_inspections/ludwig-medical-inc/7523ad0b-5079-4c50-b701-2ef670e0b4c7)
- [FDA Inspection 697474 - 2010-11-08](https://www.globalkeysolutions.net/records/fda_inspections/ludwig-medical-inc/380e79a4-819f-4473-a979-a0d55326bfd7)
- [FDA Inspection 697474 - 2010-11-08](https://www.globalkeysolutions.net/records/fda_inspections/ludwig-medical-inc/282470fa-b6dd-42de-bf84-caeacd18eb40)

Company: https://www.globalkeysolutions.net/companies/ludwig-medical-inc/a13beefc-e541-4265-be50-497bbdde68c8

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