# FDA Inspection 972177 - Maxtec, LLC. - April 01, 2016

Source: https://www.keypedia.com/records/fda_inspections/maxtec-llc/8ea3db15-34c4-4c11-b2bf-210f2e8b26d2
Source feed: FDA_Inspections

> FDA Inspection 972177 for Maxtec, LLC. on April 01, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 972177
- Company Name: Maxtec, LLC.
- Inspection Date: 2016-04-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 736970 - 2011-07-28](https://www.keypedia.com/records/fda_inspections/maxtec-llc/61ed237e-817f-4963-b34b-87ca6f1e9c75)
- [FDA Inspection 736970 - 2011-07-28](https://www.keypedia.com/records/fda_inspections/maxtec-llc/b4d73d82-659b-4638-83f1-3d17ee48955d)

Company: https://www.keypedia.com/companies/maxtec-llc/b0e24f5a-e5ed-435e-8b30-a039f3383620

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