FDA Inspection
Livingston Products, Inc.Livingston Products, Inc. – FDA Inspection, Dec 18, 2009
Record Details
This FDA Inspection record concerns Livingston Products, Inc., with an inspection on December 18, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Livingston Products, Inc.
- Inspection Date
- December 18, 2009
- Product Type
- Devices
View Company Profile
ID · 27d7e12f-65d5-48e4-ac42-1af7d27e4943
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 636157
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)(1)Uniform and timely processing
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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