# Sonoco TEQ LLC – FDA Inspection, Aug 6, 2019

Source: https://www.keypedia.com/records/fda_inspections/sonoco-teq-llc/cb57e4a1-6c8d-4403-8a14-a17d7834ed83
Source feed: FDA_Inspections

> FDA inspection 1102563 of Sonoco TEQ LLC, August 06, 2019. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102563
- Company Name: Sonoco TEQ LLC
- Inspection Date: 2019-08-06
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1315810 - 2026-05-01

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

Company: https://www.keypedia.com/companies/sonoco-teq-llc/6b2552e7-ff98-4da2-9d34-5bf56a413f97

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