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FDA Inspection
•Alfred J. Rodriguez, M.D., P.A.•February 7, 2013

Alfred J. Rodriguez, M.D., P.A. – FDA Inspection, Feb 7, 2013

Record Details

This FDA Inspection record concerns Alfred J. Rodriguez, M.D., P.A., with an inspection on February 7, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Alfred J. Rodriguez, M.D., P.A.
Inspection Date
February 7, 2013
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · a5b8647e-6e58-4e5a-9024-bb4590424c98

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
817495
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

2
  1. 21 CFR 1271.75(a)(2)Risks associated with xenotransplantation
  2. 21 CFR 1271.55(b)(3)Name and address on summary

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Alfred J. Rodriguez, M.D., P.A.

4
DateClassificationOfficeProject area
February 27, 2024VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 14, 2019NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
February 25, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 1, 2010NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Alfred J. Rodriguez, M.D., P.A.
  • FDA Inspection 1231292 - 2024-02-27
  • FDA Inspection 1080702 - 2019-02-14
  • FDA Inspection 960745 - 2016-02-25
  • FDA Inspection 679933 - 2010-09-01

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