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FDA Inspection
•Curia New Mexico, LLC•June 5, 2015

Curia New Mexico, LLC – FDA Inspection, Jun 5, 2015

Record Details

This FDA Inspection record concerns Curia New Mexico, LLC, with an inspection on June 5, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Curia New Mexico, LLC
Inspection Date
June 5, 2015
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · c77e4046-9e3c-43fa-a3a6-594f4922497b

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
929136
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

4
  1. 21 CFR 211.110(a)Control procedures to monitor and validate performance
  2. 21 CFR 211.160(b)Scientifically sound laboratory controls
  3. 21 CFR 211.192Investigations of discrepancies, failures
  4. 21 CFR 211.192Written record of investigation incomplete

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Curia New Mexico, LLC

11
DateClassificationOfficeProject area
June 28, 2024VAICenter for Drug Evaluation and ResearchNew Drug Evaluation
February 17, 2023Not classifiedDenver District Office
March 20, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 15, 2019OAIDenver District OfficeNew Drug Evaluation
December 7, 2016VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
View all 11 other inspections on the company page
Other documents for Curia New Mexico, LLC
  • FDA Inspection 1239282 - 2024-06-28
  • FDA Inspection 1200953 - 2023-02-17
  • FDA Inspection 1121293 - 2020-03-20
  • FDA Inspection 1082939 - 2019-03-15
  • FDA Inspection 999295 - 2016-12-07

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