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FDA Inspection
•J. Strickland and Co•November 20, 2025

J. Strickland and Co – FDA Inspection, Nov 20, 2025

Record Details

This FDA Inspection record concerns J. Strickland and Co, with an inspection on November 20, 2025, issued by the New Orleans District Office, covering human drugs.

Company
J. Strickland and Co
Inspection Date
November 20, 2025
Product Type
Human Drugs
Office
New Orleans District Office
Person
  • Michael Z. Weigman (Investigator)
View Company Profile

ID · 16b7233d-c70f-48b4-8184-f0a7ae928f37

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1292198
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

4
  1. 21 CFR 211.160(b)Scientifically sound laboratory controls
  2. 21 CFR 211.165(a)Testing and release for distribution
  3. 21 CFR 211.188(b)(8)Labeling control records including specimens or copies
  4. 21 CFR 211.84(d)(1)Component identity verification

Full citation text and observation details available on the Dashboard.

Other FDA inspections of J. Strickland and Co

6
DateClassificationOfficeProject area
November 23, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 27, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 26, 2014OAICenter 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 1157344 - 2021-11-23
  • FDA Inspection 982652 - 2016-05-27
  • FDA Inspection 905650 - 2014-11-26
  • FDA Inspection 842599 - 2013-08-01
  • FDA Inspection 808299 - 2012-11-15

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