# FDA Inspection 1075109 - MaxiFlex, LLC - December 20, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/maxiflex-llc/8bddc010-ba21-4efd-856d-df2f7c882351
Source feed: FDA_Inspections

> FDA Inspection 1075109 for MaxiFlex, LLC on December 20, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1075109
- Company Name: MaxiFlex, LLC
- Inspection Date: 2018-12-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1075109 - 2018-12-20](https://www.globalkeysolutions.net/records/fda_inspections/maxiflex-llc/b98fe668-b518-4493-9ea3-6023f480a652)
- [FDA Inspection 734724 - 2011-05-11](https://www.globalkeysolutions.net/records/fda_inspections/maxiflex-llc/99999132-50b3-4099-aa84-74bbcf999f01)

Company: https://www.globalkeysolutions.net/companies/maxiflex-llc/77a1952f-edeb-44bd-a2bb-b3773680959b

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