# Zeller Power Products, LLC – FDA Inspection, Jan 22, 2016

Source: https://www.keypedia.com/records/fda_inspections/zeller-power-products-llc/fd4561fe-b976-4cc6-8544-ffd766f667da
Source feed: FDA_Inspections

> FDA inspection 960780 of Zeller Power Products, LLC, January 22, 2016. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 960780
- Company Name: Zeller Power Products, LLC
- Inspection Date: 2016-01-22
- 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: 6

## Related Documents

- [FDA Inspection 1152561 - 2021-09-24](https://www.keypedia.com/records/fda_inspections/zeller-power-products-llc/c8d07333-2fd5-4f81-a19b-833c8784a48c)
- [FDA Inspection 1071492 - 2018-11-09](https://www.keypedia.com/records/fda_inspections/zeller-power-products-llc/e62b6b72-b671-4183-ab38-771ae2107f12)

Company: https://www.keypedia.com/companies/zeller-power-products-llc/c74f378e-be0a-4536-b7d7-1d5edf87fd39

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