# FDA Inspection 1013197 - Lantz Medical, Inc. - May 22, 2017

Source: https://www.keypedia.com/records/fda_inspections/lantz-medical-inc/24bce899-bb41-4a83-905e-24872e412368
Source feed: FDA_Inspections

> FDA Inspection 1013197 for Lantz Medical, Inc. on May 22, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1013197
- Company Name: Lantz Medical, Inc.
- Inspection Date: 2017-05-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1101050 - 2019-08-23](https://www.keypedia.com/records/fda_inspections/lantz-medical-inc/78112d47-1712-4b10-b7a7-7f3ee0f1634b)
- [FDA Inspection 1013197 - 2017-05-22](https://www.keypedia.com/records/fda_inspections/lantz-medical-inc/53688a26-8f48-4901-9f0a-2ab6ef20d4cc)

Company: https://www.keypedia.com/companies/lantz-medical-inc/a750fe75-aedf-4d1d-b314-17b76be54ae9

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