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FDA Inspection
•Beutlich Pharmaceuticals LLC•November 4, 2016

Beutlich Pharmaceuticals LLC – FDA Inspection, Nov 4, 2016

Record Details

This FDA Inspection record concerns Beutlich Pharmaceuticals LLC, with an inspection on November 4, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Beutlich Pharmaceuticals LLC
Inspection Date
November 4, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Ileana Barreto-Pettit (Issuing Officer)
View Company Profile

ID · e6d0ff9e-1046-485e-b8b3-8de89414f0c1

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
991891
FDA center
Human Drugs
Project area
Postmarket Surv. and Epidemiology
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 211.186(a)Written procedures followed
  2. 21 CFR 211.198(a)Complaint Handling Procedure
  3. 21 CFR 211.22(d)Procedures not in writing, fully followed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Beutlich Pharmaceuticals LLC

5
DateClassificationOfficeProject area
August 27, 2025VAIFlorida District OfficeDrug Quality Assurance
October 24, 2018VAICenter for Devices and Radiological HealthCompliance: Devices
October 29, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
March 30, 2012NAICenter for Devices and Radiological HealthCompliance: Devices
February 22, 2011NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
Other documents for Beutlich Pharmaceuticals LLC
  • FDA Inspection 1279681 - 2025-08-27
  • FDA Inspection 1069715 - 2018-10-24
  • FDA Inspection 946582 - 2015-10-29
  • FDA Inspection 773041 - 2012-03-30
  • FDA Inspection 716447 - 2011-02-22

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