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FDA Inspection
•Time-Cap Laboratories, Inc.•December 18, 2019

Time-Cap Laboratories, Inc. – FDA Inspection, Dec 18, 2019

Record Details

This FDA Inspection record concerns Time-Cap Laboratories, Inc., with an inspection on December 18, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Time-Cap Laboratories, Inc.
Inspection Date
December 18, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 744d147b-2950-4c47-8812-f001f573a7bb

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1113101
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

3
  1. 21 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
  2. 21 CFR 211.192Investigations of discrepancies, failures
  3. 21 CFR 211.22(d)Procedures not in writing, fully followed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Time-Cap Laboratories, Inc.

12
DateClassificationOfficeProject area
April 24, 2025VAINew York District OfficeDrug Quality Assurance
October 10, 2023NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
March 12, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 10, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 16, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 12 other inspections on the company page
Other documents for Time-Cap Laboratories, Inc.
  • FDA Inspection 1263597 - 2025-04-24
  • FDA Inspection 1221504 - 2023-10-10
  • FDA Inspection 1043706 - 2018-03-12
  • FDA Inspection 963304 - 2016-03-10
  • FDA Inspection 909667 - 2015-01-16

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