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483
•Lovelace Biomedical Research Institute•September 13, 2019

FDA 483 - Lovelace Biomedical Research Institute - September 13, 2019

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Record Details

Lovelace Respiratory Research Institute was cited for deficiencies in assuring data integrity and maintaining quality assurance during nonclinical laboratory studies. The inspection revealed that the study director failed to ensure accurate recording and verification of experimental data, specifically regarding test article preparation. Furthermore, the quality assurance unit did not maintain a complete master schedule for all nonclinical laboratory studies.

Company
Lovelace Biomedical Research Institute
Inspection Date
September 13, 2019
Product Type
Other
Office
Denver District Office
People
  • Zhou Chen (issuing_officer)
  • Jeanne J. Thai (investigator)
  • Dustin Tran (Investigator )
  • Ruth A. Williams (issuing_officer)
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ID · 2cc69e59-a746-45c0-8ae0-e016b5b84b9e

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