FDA inspection

New Hampshire Processing Facility: FDA inspection ending Feb 17, 2000

FDA inspection 14838 · No Action Indicated (NAI) · Portsmouth, NH

Key facts

Inspection ID	14838
Firm	New Hampshire Processing Facility
FEI number	3000202850
Address	875 Greenland Rd Unit C3
City	Portsmouth
State	NH
ZIP	03801-4163
Fiscal year	2000
Inspection end date	Feb 17, 2000
Classification	No Action Indicated (NAI)
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
None 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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