# FDA Inspection 1315810 - Sonoco TEQ LLC - May 01, 2026

Source: https://www.keypedia.com/records/fda_inspections/sonoco-teq-llc/9a5e6dc3-46f2-4c2b-81be-f29a2b1d71fa
Source feed: FDA_Inspections

> FDA Inspection 1315810 for Sonoco TEQ LLC on May 01, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1315810
- Company Name: Sonoco TEQ LLC
- Inspection Date: 2026-05-01
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1315810 - 2026-05-01](https://www.keypedia.com/records/fda_inspections/sonoco-teq-llc/7bbabef4-acd8-41db-b91a-be3872c5cc72)
- [FDA Inspection 1102563 - 2019-08-06](https://www.keypedia.com/records/fda_inspections/sonoco-teq-llc/cb57e4a1-6c8d-4403-8a14-a17d7834ed83)

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