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FDA Inspection
•Techni Med, Inc. dba The Compounder•October 10, 2019

Techni Med, Inc. dba The Compounder – FDA Inspection, Oct 10, 2019

Record Details

This FDA Inspection record concerns Techni Med, Inc. dba The Compounder, with an inspection on October 10, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Techni Med, Inc. dba The Compounder
Inspection Date
October 10, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 32619836-93e0-4a21-bf04-44facdfd64ee

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1106708
FDA center
Human Drugs
Project area
Drug Quality Assurance
Enforcement
State Referral Letter

FDA Citations

4
  1. Non-microbial contamination, production area
  2. 21 CFR 211.165(a)Testing and release for distribution
  3. Actionable microbial contamination, adjacent area
  4. Use of non-pharmaceutical grade components

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Techni Med, Inc. dba The Compounder

2
DateClassificationOfficeProject area
January 26, 2018OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 9, 2015OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Techni Med, Inc. dba The Compounder
  • FDA Inspection 1041122 - 2018-01-26
  • FDA Inspection 933301 - 2015-07-09

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