# FDA Inspection 1109221 - Linatech, Llc - November 08, 2019

Source: https://www.keypedia.com/records/fda_inspections/linatech-llc/bf794fae-91c3-4827-9f07-16c2ac60c871
Source feed: FDA_Inspections

> FDA Inspection 1109221 for Linatech, Llc on November 08, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1109221
- Company Name: Linatech, Llc
- Inspection Date: 2019-11-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1153839 - 2021-09-29](https://www.keypedia.com/records/fda_inspections/linatech-llc/5c9716d6-15e0-43e6-9b3b-75b907aaf893)
- [FDA Inspection 1109221 - 2019-11-08](https://www.keypedia.com/records/fda_inspections/linatech-llc/893ebbae-0416-4053-85e7-f9ed4b7e9f9c)

Company: https://www.keypedia.com/companies/linatech-llc/ad0444d9-c00d-47a2-9bb7-e94dde896bc9

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