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FDA Inspection
•G. C. Hanford Manufacturing Co•November 30, 2012

G. C. Hanford Manufacturing Co – FDA Inspection, Nov 30, 2012

Record Details

This FDA Inspection record concerns G. C. Hanford Manufacturing Co, with an inspection on November 30, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
G. C. Hanford Manufacturing Co
Inspection Date
November 30, 2012
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 2b69f6e1-3319-4199-87d2-c43eaed7b311

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
808118
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

1
  1. 21 CFR 211.22(d)Procedures not in writing, fully followed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of G. C. Hanford Manufacturing Co

18
DateClassificationOfficeProject area
March 20, 2025OAINew York District OfficeDrug Quality Assurance
June 17, 2022VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
September 27, 2019VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
September 27, 2019VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
December 16, 2016VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
View all 18 other inspections on the company page
Other documents for G. C. Hanford Manufacturing Co
  • FDA Inspection 1264589 - 2025-03-20
  • FDA Inspection 1172077 - 2022-06-17
  • FDA Inspection 1102963 - 2019-09-27
  • FDA Inspection 1102962 - 2019-09-27
  • FDA Inspection 999137 - 2016-12-16

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