# Spellman Hg Vltg Elctrnc – FDA Inspection, Apr 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/spellman-hg-vltg-elctrnc/d7ef9ac6-0e11-49be-b597-c192db919dfb
Source feed: FDA_Inspections

> FDA inspection 1012034 of Spellman Hg Vltg Elctrnc, April 26, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1012034
- Company Name: Spellman Hg Vltg Elctrnc
- Inspection Date: 2017-04-26
- 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: 1

## Related Documents

- FDA Inspection 867057 - 2014-02-21
- FDA Inspection 777937 - 2012-04-17
- FDA Inspection 639308 - 2010-01-15

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/andrew-j-garufi/567f6aaa-f6f2-45a3-9a58-80b33f3ad021)

Company: https://www.keypedia.com/companies/spellman-hg-vltg-elctrnc/6926367a-98c7-44a7-bd0a-3b83aea7c5dc

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