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FDA Inspection
•J. Strickland and Co•November 26, 2014

J. Strickland and Co – FDA Inspection, Nov 26, 2014

Record Details

This FDA Inspection record concerns J. Strickland and Co, with an inspection on November 26, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
J. Strickland and Co
Inspection Date
November 26, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 599e15b7-07ca-493f-8487-61b86861c2da

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
905650
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

19
  1. 21 CFR 211.103Actual vs. theoretical yields not determined
  2. 21 CFR 211.188Prepared for each batch, include complete information
  3. 21 CFR 211.110(a)Control procedures to monitor and validate performance
  4. 21 CFR 211.100(b)Procedure Deviations Recorded and Justified
  5. 21 CFR 211.160(a)Deviations from laboratory control requirements
  6. 21 CFR 211.142(a)Quarantine - actual practice
  7. 21 CFR 211.137(a)Expiration date lacking
  8. 21 CFR 211.25(a)Training , Education , Experience overall
  9. 21 CFR 211.25(b)Supervisor Training/Education/Experience
  10. 21 CFR 211.160(b)Scientifically sound laboratory controls

Showing 10 of 19 citations.

Full citation text and observation details available on the Dashboard.

Other FDA inspections of J. Strickland and Co

6
DateClassificationOfficeProject area
November 20, 2025VAINew Orleans District OfficeDrug Quality Assurance
November 23, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 27, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 1, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 15, 2012OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for J. Strickland and Co
  • FDA Inspection 1292198 - 2025-11-20
  • FDA Inspection 1157344 - 2021-11-23
  • FDA Inspection 982652 - 2016-05-27
  • FDA Inspection 842599 - 2013-08-01
  • FDA Inspection 808299 - 2012-11-15

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