FDA Inspection
Vitalitec International, Inc.Vitalitec International, Inc. – FDA Inspection, Jul 19, 2013
Record Details
This FDA Inspection record concerns Vitalitec International, Inc., with an inspection on July 19, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- July 19, 2013
- Product Type
- Devices
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ID · fc1da518-73cf-45c2-a62f-b94ddec7d5ce
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 843178
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.40(a)Not approved or obsolete document retrieval
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