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FDA Inspection
•Identipak Inc•December 18, 2025

FDA Inspection 1295928 - Identipak Inc - December 18, 2025

Record Details

This FDA Inspection record concerns Identipak Inc, with an inspection on December 18, 2025, issued by the Dallas District Office, covering human drugs.

Company
Identipak Inc
Inspection Date
December 18, 2025
Product Type
Human Drugs
Office
Dallas District Office
Person
  • Rodney L. Tinzie
View Company Profile

ID · fad91f1a-976f-4b81-9693-1fed04be2490

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1295928
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

3
  1. 21 CFR 211.180(e)(1)Review of representative number of batches
  2. 21 CFR 211.67(b)(3)Cleaning SOPs/instructions
  3. 21 CFR 211.67(c)Cleaning/maintenance records not kept

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Identipak Inc

3
DateClassificationOfficeProject area
June 5, 2025Not classifiedDallas District Office
June 8, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 22, 2011NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
Other documents for Identipak Inc
  • FDA Inspection 1273428 - 2025-06-05
  • FDA Inspection 971718 - 2016-06-08
  • FDA Inspection 732573 - 2011-06-22

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