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FDA Inspection
•Allermed Laboratories, LLC•June 14, 2017

Allermed Laboratories, LLC – FDA Inspection, Jun 14, 2017

Record Details

This FDA Inspection record concerns Allermed Laboratories, LLC, with an inspection on June 14, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Allermed Laboratories, LLC
Inspection Date
June 14, 2017
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Simone E. Pitts (FDA Associated Person)
View Company Profile

ID · 66fae5e0-e58b-4b28-9805-47f77f352004

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1022877
FDA center
Biologics
Project area
Vaccines and Allergenic Products
Outcome
Form 483 issued

Other FDA inspections of Allermed Laboratories, LLC

6
DateClassificationOfficeProject area
January 31, 2024VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
November 12, 2018VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
July 13, 2015VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
August 12, 2013VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
September 27, 2011VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
View all 6 other inspections on the company page
Other documents for Allermed Laboratories, LLC
  • FDA Inspection 1228221 - 2024-01-31
  • FDA Inspection 1071500 - 2018-11-12
  • FDA Inspection 933388 - 2015-07-13
  • FDA Inspection 843070 - 2013-08-12
  • FDA Inspection 749646 - 2011-09-27

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