# FDA Inspection 1012034 - Spellman Hg Vltg Elctrnc - April 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 for Spellman Hg Vltg Elctrnc on April 26, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1012034 - 2017-04-26](https://www.keypedia.com/records/fda_inspections/spellman-hg-vltg-elctrnc/6d2afdd9-4d59-4ede-a77e-946c26170463)
- [FDA Inspection 867057 - 2014-02-21](https://www.keypedia.com/records/fda_inspections/spellman-hg-vltg-elctrnc/c2f33989-b8bc-40ba-8b3a-94a8a61113a1)
- [FDA Inspection 867057 - 2014-02-21](https://www.keypedia.com/records/fda_inspections/spellman-hg-vltg-elctrnc/428ea8b9-5c1e-4512-8fc9-434c01506890)
- [FDA Inspection 777937 - 2012-04-17](https://www.keypedia.com/records/fda_inspections/spellman-hg-vltg-elctrnc/2e801398-1b54-44ce-a33a-8153d8cd66da)
- [FDA Inspection 777937 - 2012-04-17](https://www.keypedia.com/records/fda_inspections/spellman-hg-vltg-elctrnc/7b3f085d-f067-4759-bd74-4d1c2168fefe)

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