# FDA Inspection 1102929 - Primotec LLC - September 25, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/primotec-llc/6a84dac0-dca3-4610-8252-19fdd598e98b
Source feed: FDA_Inspections

> FDA Inspection 1102929 for Primotec LLC on September 25, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102929
- Company Name: Primotec LLC
- Inspection Date: 2019-09-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1102929 - 2019-09-25](https://www.globalkeysolutions.net/records/fda_inspections/primotec-llc/de0c1633-3d18-4d1d-909f-e9acae97e6d3)

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

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