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FDA Inspection
•Kaiser Permanente-Sunnyside Medical Center•December 4, 2014

Kaiser Permanente-Sunnyside Medical Center – FDA Inspection, Dec 4, 2014

Record Details

This FDA Inspection record concerns Kaiser Permanente-Sunnyside Medical Center, with an inspection on December 4, 2014, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Kaiser Permanente-Sunnyside Medical Center
Inspection Date
December 4, 2014
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 055ec355-a71e-4f56-abf2-22f9cede3d8b

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
905708
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

2
  1. 21 CFR 606.60(a)Maintain and clean equipment
  2. 21 CFR 606.160(a)(1)Concurrent documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Kaiser Permanente-Sunnyside Medical Center

7
DateClassificationOfficeProject area
March 11, 2025Not classifiedSeattle District Office
December 7, 2021NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
July 31, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
November 2, 2016VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 13, 2013VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 7 other inspections on the company page
Other documents for Kaiser Permanente-Sunnyside Medical Center
  • FDA Inspection 1263925 - 2025-03-11
  • FDA Inspection 1158929 - 2021-12-07
  • FDA Inspection 1061266 - 2018-07-31
  • FDA Inspection 995641 - 2016-11-02
  • FDA Inspection 819227 - 2013-02-13

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