FDA Inspection
VitalWear Inc.VitalWear Inc. – FDA Inspection, Dec 15, 2010
Record Details
This FDA Inspection record concerns VitalWear Inc., with an inspection on December 15, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- VitalWear Inc.
- Inspection Date
- December 15, 2010
- Product Type
- Devices
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ID · 830aca1b-81bc-4951-81f5-48633729f622
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 701967
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.250(b)Sampling methods - Lack of or inadequate procedures
- 21 CFR 820.70(a)Production processes
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Other FDA inspections of VitalWear Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 23, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 3, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for VitalWear Inc.
- FDA Inspection 829679 - 2013-04-23
- FDA Inspection 665970 - 2010-06-03
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