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FDA Inspection
•OLAX Corp.•August 1, 2017

OLAX Corp. – FDA Inspection, Aug 1, 2017

Record Details

This FDA Inspection record concerns OLAX Corp., with an inspection on August 1, 2017, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
OLAX Corp.
Inspection Date
August 1, 2017
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
Person
  • David P. King (Issuing Officer)
View Company Profile

ID · 747aebc0-9683-4bdd-ae45-9e6a024f6384

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1020028
FDA center
Foods & Cosmetics
Project area
Food Composition, Standards, Labeling and Econ
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 111.153Written procedures - product received; packaging, labeling
  2. 21 CFR 111.255(a)Batch record - every batch
  3. 21 CFR 111.205(a)Master manufacturing record - each batch

Full citation text and observation details available on the Dashboard.

Other FDA inspections of OLAX Corp.

3
DateClassificationOfficeProject area
December 9, 2025Not classifiedFlorida District Office
December 10, 2013VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
February 4, 2013OAICenter for Drug Evaluation and ResearchUnapproved and Misbranded Drugs
Other documents for OLAX Corp.
  • FDA Inspection 1229287 - 2025-12-09
  • FDA Inspection 858675 - 2013-12-10
  • FDA Inspection 817363 - 2013-02-04

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