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FDA Inspection
•Tjoapack Netherlands BV•May 25, 2018

Tjoapack Netherlands BV – FDA Inspection, May 25, 2018

Record Details

This FDA Inspection record concerns Tjoapack Netherlands BV, with an inspection on May 25, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Tjoapack Netherlands BV
Inspection Date
May 25, 2018
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Burnell M. Henry (FDA Associated Person)
View Company Profile

ID · 4858c333-f54e-4cc6-aaa5-40ae0bfdc75c

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1059654
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

Other FDA inspections of Tjoapack Netherlands BV

1
DateClassificationOfficeProject area
June 14, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Tjoapack Netherlands BV
  • FDA Inspection 1204462 - 2022-06-14

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