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FDA Inspection
•Frances Mahon Deaconess Hospital•July 15, 2009

Frances Mahon Deaconess Hospital – FDA Inspection, Jul 15, 2009

Record Details

This FDA Inspection record concerns Frances Mahon Deaconess Hospital, with an inspection on July 15, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Frances Mahon Deaconess Hospital
Inspection Date
July 15, 2009
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 4c32d408-ac57-411b-89ed-cc81deec090e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
613717
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

3
  1. 21 CFR 606.60(a)Equipment observed, standardized, calibrated
  2. 21 CFR 606.160(b)Required records
  3. 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Frances Mahon Deaconess Hospital

10
DateClassificationOfficeProject area
June 8, 2026Not classifiedSeattle District Office
May 6, 2025Not classifiedSeattle District Office
May 8, 2024Not classifiedSeattle District Office
May 18, 2023Not classifiedSeattle District Office
September 13, 2019Not classifiedSeattle District Office
View all 10 other inspections on the company page
Other documents for Frances Mahon Deaconess Hospital
  • FDA Inspection 1322728 - 2026-06-08
  • FDA Inspection 1269981 - 2025-05-06
  • FDA Inspection 1238875 - 2024-05-08
  • FDA Inspection 1213697 - 2023-05-18
  • FDA Inspection 1104367 - 2019-09-13

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