# Enviropak LLC – FDA Inspection, Jul 11, 2018

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

> FDA inspection 1058918 of Enviropak LLC, July 11, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1058918
- Company Name: Enviropak LLC
- Inspection Date: 2018-07-11
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1337046 - 2026-09-23](https://www.keypedia.com/records/fda_inspections/enviropak-llc/9b09b64a-6ab0-4146-b255-2aecd18c4440)
- FDA Inspection 915736 - 2015-02-24

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sayeeda-hdabe/eaadc7cf-5f22-47c2-ba02-437efe0a5267)

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

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