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FDA Inspection
•MaxPax, LLC•June 24, 2015

MaxPax, LLC – FDA Inspection, Jun 24, 2015

Record Details

This FDA Inspection record concerns MaxPax, LLC, with an inspection on June 24, 2015, issued by the Center for Veterinary Medicine, covering veterinary.

Company
MaxPax, LLC
Inspection Date
June 24, 2015
Product Type
Veterinary
Office
Center for Veterinary Medicine
View Company Profile

ID · f2d62830-1c8f-46f0-b8e7-61a7eaa040fd

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
931181
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices

FDA Citations

6
  1. 21 CFR 211.84(d)(2)Establish reliability of supplier"s C of A
  2. 21 CFR 211.160(b)Scientifically sound laboratory controls
  3. 21 CFR 211.100(a)Absence of Written Procedures
  4. 21 CFR 211.166(a)Lack of written stability program
  5. 21 CFR 211.22(d)Procedures not in writing, fully followed
  6. 21 CFR 211.67(b)Written procedures not established/followed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of MaxPax, LLC

5
DateClassificationOfficeProject area
July 25, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 11, 2014VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
January 14, 2013VAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
October 31, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 14, 2009VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
Other documents for MaxPax, LLC
  • FDA Inspection 1097437 - 2019-07-25
  • FDA Inspection 885213 - 2014-07-11
  • FDA Inspection 814003 - 2013-01-14
  • FDA Inspection 752375 - 2011-10-31
  • FDA Inspection 604502 - 2009-08-14

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