FDA Inspection 1204268 — IDB Holland B.V.

IDB Holland B.V. — FEI 3010293768

The FDA completed an inspection of IDB Holland B.V. on Jan 12, 2022 in Baarle-Nassau. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 12, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Baarle-Nassau (Netherlands)

Additional Details

Mutual Recognition Agreement (MRA)

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