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FDA Inspection
•ALS Group USA Corp•February 6, 2017

ALS Group USA Corp – FDA Inspection, Feb 6, 2017

Record Details

This FDA Inspection record concerns ALS Group USA Corp, with an inspection on February 6, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
ALS Group USA Corp
Inspection Date
February 6, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Camerson E. Moore (FDA Associated Person)
View Company Profile

ID · a806e824-bff0-4b4f-b486-ca14d59242ee

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1009089
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 211.194(a)(8)Second person sign off
  2. 21 CFR 211.182Personnel dating/signing equipment log

Full citation text and observation details available on the Dashboard.

Other FDA inspections of ALS Group USA Corp

1
DateClassificationOfficeProject area
March 23, 2022NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for ALS Group USA Corp
  • FDA Inspection 1166549 - 2022-03-23

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