# Ziptek LLC – FDA Inspection, May 8, 2018

Source: https://www.keypedia.com/records/fda_inspections/ziptek-llc/d14a63ed-9f35-425c-a7df-97eb603686bf
Source feed: FDA_Inspections

> FDA inspection 1051750 of Ziptek LLC, May 08, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1051750
- Company Name: Ziptek LLC
- Inspection Date: 2018-05-08
- 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: 4

## Related Documents

- [FDA Inspection 1239943 - 2024-05-22](https://www.keypedia.com/records/fda_inspections/ziptek-llc/f6034f87-e55d-41f1-9755-929422b45ca2)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/richard-k-vogel/3ddd8bff-24fd-40ee-b0a7-fb5333a520f5)

Company: https://www.keypedia.com/companies/ziptek-llc/ce6d62bc-fc2e-43c5-afc4-79a3c40d5b4c

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