FDA Inspection
Spellman Hg Vltg ElctrncSpellman Hg Vltg Elctrnc – FDA Inspection, Apr 26, 2017
Record Details
This FDA Inspection record concerns Spellman Hg Vltg Elctrnc, with an inspection on April 26, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d7ef9ac6-0e11-49be-b597-c192db919dfb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1012034
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.100(b)Documentation
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Other FDA inspections of Spellman Hg Vltg Elctrnc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 21, 2014 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| April 17, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 15, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Spellman Hg Vltg Elctrnc
- FDA Inspection 867057 - 2014-02-21
- FDA Inspection 777937 - 2012-04-17
- FDA Inspection 639308 - 2010-01-15
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