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FDA Inspection
•RLC Labs Inc.•November 2, 2023

RLC Labs Inc. – FDA Inspection, Nov 2, 2023

Record Details

This FDA Inspection record concerns RLC Labs Inc., with an inspection on November 2, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
RLC Labs Inc.
Inspection Date
November 2, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Cecilia H. Kieu (FDA Associated Person)
View Company Profile

ID · 6faef532-a668-4623-aafd-6a78800a9ce3

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1221698
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 211.22(a)Approve or reject components, products
  2. 21 CFR 211.22(a)Approve or reject components, products

Full citation text and observation details available on the Dashboard.

Other FDA inspections of RLC Labs Inc.

5
DateClassificationOfficeProject area
November 4, 2021OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 11, 2017VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
February 8, 2012NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 15, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 26, 2009NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for RLC Labs Inc.
  • FDA Inspection 1156014 - 2021-11-04
  • FDA Inspection 1021606 - 2017-08-11
  • FDA Inspection 766950 - 2012-02-08
  • FDA Inspection 703127 - 2010-12-15
  • FDA Inspection 564408 - 2009-01-26

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