# FDA Inspection 734724 - MaxiFlex, LLC - May 11, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/maxiflex-llc/99999132-50b3-4099-aa84-74bbcf999f01
Source feed: FDA_Inspections

> FDA Inspection 734724 for MaxiFlex, LLC on May 11, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 734724
- Company Name: MaxiFlex, LLC
- Inspection Date: 2011-05-11
- Classification: No Action Indicated (NAI)
- 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/8bddc010-ba21-4efd-856d-df2f7c882351)
- [FDA Inspection 1075109 - 2018-12-20](https://www.globalkeysolutions.net/records/fda_inspections/maxiflex-llc/b98fe668-b518-4493-9ea3-6023f480a652)

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