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FDA Inspection
•Albert Max, Inc.•May 25, 2017

Albert Max, Inc. – FDA Inspection, May 25, 2017

Record Details

This FDA Inspection record concerns Albert Max, Inc., with an inspection on May 25, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Albert Max, Inc.
Inspection Date
May 25, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Marcus F. Yambot (FDA Associated Person)
View Company Profile

ID · 0dffa158-6426-43a7-9712-e9cec50a3729

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1014057
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 211.160(b)Scientifically sound laboratory controls
  2. 21 CFR 211.22(a)Contract drug products--lack of responsibility

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Albert Max, Inc.

5
DateClassificationOfficeProject area
June 11, 2026VAILos Angeles District OfficeFoodborne Biological Hazards
April 15, 2021NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
September 16, 2016VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
May 28, 2013OAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
May 19, 2009NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Albert Max, Inc.
  • FDA Inspection 1321612 - 2026-06-11
  • FDA Inspection 1142624 - 2021-04-15
  • FDA Inspection 989423 - 2016-09-16
  • FDA Inspection 833396 - 2013-05-28
  • FDA Inspection 584290 - 2009-05-19

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