# Primotec LLC – FDA Inspection, Sep 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/primotec-llc/de0c1633-3d18-4d1d-909f-e9acae97e6d3
Source feed: FDA_Inspections

> FDA inspection 1102929 of Primotec LLC, September 25, 2019. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102929
- Company Name: Primotec LLC
- Inspection Date: 2019-09-25
- 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 Officers

- [Company Rep](https://www.keypedia.com/people/michael-g-mayfield/ec045e12-d940-4f76-a17f-98ba4a8dd5b9)

Company: https://www.keypedia.com/companies/primotec-llc/e12f5561-ce4c-48c6-b00c-1b5efa453b23

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