# Tjoapack Netherlands BV – FDA Inspection, May 25, 2018

Source: https://www.keypedia.com/records/fda_inspections/tjoapack-netherlands-bv/4858c333-f54e-4cc6-aaa5-40ae0bfdc75c
Source feed: FDA_Inspections

> FDA inspection 1059654 of Tjoapack Netherlands BV, May 25, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1059654
- Company Name: Tjoapack Netherlands BV
- Inspection Date: 2018-05-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Center: Biologics
- Office Name: Center for Biologics Evaluation and Research
- Citation Count: 0

## Related Documents

- FDA Inspection 1204462 - 2022-06-14

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/burnell-m-henry/dece4407-3597-4a58-8756-5abf9db43bbc)

Company: https://www.keypedia.com/companies/tjoapack-netherlands-bv/597a0eff-cdc4-4794-be52-7ba5ccda3ba7

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d