FDA Inspection
J. LOZADA DISTRIBUTORSJ. LOZADA DISTRIBUTORS – FDA Inspection, Oct 11, 2012
Record Details
This FDA Inspection record concerns J. LOZADA DISTRIBUTORS, with an inspection on October 11, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- J. LOZADA DISTRIBUTORS
- Inspection Date
- October 11, 2012
- Product Type
- Devices
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ID · 888bfaab-9286-4252-8b5c-70d4043b25cd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 802725
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
3- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.150Lack of or inadequate procedures for storage.
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