# MaxiFlex, LLC – FDA Inspection, Dec 20, 2018

Source: https://www.keypedia.com/records/fda_inspections/maxiflex-llc/b98fe668-b518-4493-9ea3-6023f480a652
Source feed: FDA_Inspections

> FDA inspection 1075109 of MaxiFlex, LLC, December 20, 2018. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1075109
- Company Name: MaxiFlex, LLC
- Inspection Date: 2018-12-20
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 734724 - 2011-05-11

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/wanda-b-coats/093122f7-c3af-42f7-a2c8-baf35313d797)

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

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