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FDA Inspection
•Cleveland Clinic Mercy Hospital•November 30, 2012

Cleveland Clinic Mercy Hospital – FDA Inspection, Nov 30, 2012

Record Details

This FDA Inspection record concerns Cleveland Clinic Mercy Hospital, with an inspection on November 30, 2012, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Cleveland Clinic Mercy Hospital
Inspection Date
November 30, 2012
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 2da39dde-e85f-4f22-80cf-32062762a519

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
808837
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

1
  1. 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 Cleveland Clinic Mercy Hospital

7
DateClassificationOfficeProject area
April 25, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 17, 2022NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
October 11, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
October 25, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
October 21, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 7 other inspections on the company page
Other documents for Cleveland Clinic Mercy Hospital
  • FDA Inspection 1238101 - 2024-04-25
  • FDA Inspection 1163363 - 2022-02-17
  • FDA Inspection 1070001 - 2018-10-11
  • FDA Inspection 988944 - 2016-10-25
  • FDA Inspection 900582 - 2014-10-21

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