# FDA Inspection 979543 - Sonoco Plastics B.V - June 30, 2016

Source: https://www.keypedia.com/records/fda_inspections/sonoco-plastics-bv/5fd48f60-36a0-43ad-8e43-4edeb0cc911c
Source feed: FDA_Inspections

> FDA Inspection 979543 for Sonoco Plastics B.V on June 30, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 979543
- Company Name: Sonoco Plastics B.V
- Inspection Date: 2016-06-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1101658 - 2019-08-22](https://www.keypedia.com/records/fda_inspections/sonoco-plastics-bv/3a740e64-a4e7-4f56-a9a4-6830c39b163d)
- [FDA Inspection 979543 - 2016-06-30](https://www.keypedia.com/records/fda_inspections/sonoco-plastics-bv/4526f698-5f0b-4ab7-b270-f2951820f639)

Company: https://www.keypedia.com/companies/sonoco-plastics-bv/142ef1c6-b7ff-4dad-9499-cb4acb719362

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