# FDA Inspection 1058918 - Enviropak LLC - July 11, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/enviropak-llc/89704c75-dce6-4a99-9573-409243e6a855
Source feed: FDA_Inspections

> FDA Inspection 1058918 for Enviropak LLC on July 11, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1058918
- Company Name: Enviropak LLC
- Inspection Date: 2018-07-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 915736 - 2015-02-24](https://www.globalkeysolutions.net/records/fda_inspections/enviropak-llc/d9b0a5f7-6588-464f-bba8-793af338523c)
- [FDA Inspection 915736 - 2015-02-24](https://www.globalkeysolutions.net/records/fda_inspections/enviropak-llc/f235a511-4a9e-4dc4-a6d0-aab53ecdd532)

Company: https://www.globalkeysolutions.net/companies/enviropak-llc/12e0df4f-a353-4f07-aeb8-3a3d508428c1

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