FDA inspection

Zlb Bioplasma, Inc: FDA inspection ending Aug 20, 2001

FDA inspection 84332 · Voluntary Action Indicated (VAI) · Detroit, MI

Key facts

Inspection ID	84332
Firm	Zlb Bioplasma, Inc
FEI number	1832353
Address	15240 Grand River Ave
City	Detroit
State	MI
ZIP	48227
Fiscal year	2001
Inspection end date	Aug 20, 2001
Classification	Voluntary Action Indicated (VAI)
Project area	Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood & Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products\|Blood and Blood Products
Product type	Biologics

At a glance

None Citations
1–9 Posted citations
No Warning letter followed
Yes Form FDA 483 issued
No Establishment inspection report (EIR) exists
1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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