# Maxtec, LLC. – FDA Inspection, Apr 1, 2016

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

> FDA inspection 972177 of Maxtec, LLC., April 01, 2016. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 736970 - 2011-07-28

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