# FDA Inspection 1023513 - Westrock Converting Company LLC - July 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/westrock-converting-company-llc/41ae5bf6-6c50-4541-951d-7641c9649d78
Source feed: FDA_Inspections

> FDA Inspection 1023513 for Westrock Converting Company LLC on July 20, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023513
- Company Name: Westrock Converting Company LLC
- Inspection Date: 2017-07-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/westrock-converting-company-llc/8cd46e91-6408-4bad-9c0f-86d58c2f196e

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