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FDA Inspection
•Greenco Industries, Inc.•April 8, 2014

Greenco Industries, Inc. – FDA Inspection, Apr 8, 2014

Record Details

This FDA Inspection record concerns Greenco Industries, Inc., with an inspection on April 8, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Greenco Industries, Inc.
Inspection Date
April 8, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 4666ad26-0e0f-4729-b74d-66b82aec2203

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
874497
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

4
  1. 21 CFR 211.22(a)Contract drug products--lack of responsibility
  2. 21 CFR 211.22(c)Approve or reject procedures or specs
  3. 21 CFR 211.100(a)Absence of Written Procedures
  4. 21 CFR 211.166(a)Lack of written stability program

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Greenco Industries, Inc.

4
DateClassificationOfficeProject area
December 17, 2025NAIFoodborne Biological Hazards
December 11, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 2, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 14, 2009NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Greenco Industries, Inc.
  • FDA Inspection 1300148 - 2025-12-17
  • FDA Inspection 1076624 - 2018-12-11
  • FDA Inspection 781910 - 2012-05-02
  • FDA Inspection 597358 - 2009-07-14

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