FDA inspection

Lakes Region Obgyn, Pa: FDA inspection ending Nov 12, 2003

FDA inspection 305569 · No Action Indicated (NAI) · Laconia, NH

Key facts

Inspection ID 305569
Firm Lakes Region Obgyn, Pa
FEI number 1000513612
Address 96 High St
City Laconia
State NH
ZIP 03246-3537
Fiscal year 2004
Inspection end date Nov 12, 2003
Classification No Action Indicated (NAI)
Project area Mammography Qual Stand Act (MQSA) Auth
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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