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FDA Inspection
•Consumer Product Partners, LLC•January 11, 2017

Consumer Product Partners, LLC – FDA Inspection, Jan 11, 2017

Record Details

This FDA Inspection record concerns Consumer Product Partners, LLC, with an inspection on January 11, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Consumer Product Partners, LLC
Inspection Date
January 11, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Tiara N Brown-Crosen (Issuing Officer)
View Company Profile

ID · a3d4fe65-6ad0-4329-9660-0246fac27f9f

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
997500
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 211.68(b)Computer control of master formula records
  2. 21 CFR 211.67(b)Written procedures not established/followed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Consumer Product Partners, LLC

7
DateClassificationOfficeProject area
February 5, 2026Not classifiedKansas City District OfficeDrug Quality Assurance
February 29, 2024NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
June 14, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 13, 2021OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 13, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Consumer Product Partners, LLC
  • FDA Inspection 1297262 - 2026-02-05
  • FDA Inspection 1231898 - 2024-02-29
  • FDA Inspection 1208351 - 2023-06-14
  • FDA Inspection 1155148 - 2021-10-13
  • FDA Inspection 954647 - 2016-01-13

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Contact
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