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FDA Inspection
•Lifetech Resources, LLC•March 3, 2025

Lifetech Resources, LLC – FDA Inspection, Mar 3, 2025

Record Details

This FDA Inspection record concerns Lifetech Resources, LLC, with an inspection on March 3, 2025, issued by the Los Angeles District Office, covering human drugs.

Company
Lifetech Resources, LLC
Inspection Date
March 3, 2025
Product Type
Human Drugs
Office
Los Angeles District Office
Person
  • Christopher R. Czajka (FDA Associated Person)
View Company Profile

ID · b49242ed-a567-4a6f-a939-1da334bf894f

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1262598
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

4
  1. 21 CFR 211.142(b)Storage under appropriate conditions
  2. 21 CFR 211.25(a)Training--operations, GMPs, written procedures
  3. 21 CFR 211.125(a)Strict control not exercised over labeling issued
  4. 21 CFR 211.170(a)Reserve sample quantity - active ingredients only

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Lifetech Resources, LLC

4
DateClassificationOfficeProject area
April 5, 2019VAICenter for Drug Evaluation and ResearchUnapproved and Misbranded Drugs
September 3, 2014OAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
February 2, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 27, 2010OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Lifetech Resources, LLC
  • FDA Inspection 1086572 - 2019-04-05
  • FDA Inspection 894309 - 2014-09-03
  • FDA Inspection 766174 - 2012-02-02
  • FDA Inspection 683143 - 2010-09-27

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