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FDA Inspection
•Paket Corp•April 10, 2025

Paket Corp – FDA Inspection, Apr 10, 2025

Record Details

This FDA Inspection record concerns Paket Corp, with an inspection on April 10, 2025, issued by the Chicago District Office, covering human drugs.

Company
Paket Corp
Inspection Date
April 10, 2025
Product Type
Human Drugs
Office
Chicago District Office
Person
  • Tyler M. Peterson (Issuing Officer)
View Company Profile

ID · bde5a82b-9b7c-4e51-9834-749e717bbbcb

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1266580
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

2
  1. 21 CFR 211.25(c)Inadequate number of personnel
  2. 21 CFR 211.67(b)Written procedures not established/followed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Paket Corp

2
DateClassificationOfficeProject area
August 6, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 31, 2017Not classifiedChicago District Office
Other documents for Paket Corp
  • FDA Inspection 1098750 - 2019-08-06
  • FDA Inspection 1005578 - 2017-03-31

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