FDA inspection

Bluffton Hlth Systems LLC dba Bluffton Regional Med Ctr: FDA inspection ending Nov 23, 1999

FDA inspection 5001 · No Action Indicated (NAI) · Bluffton, IN

Key facts

Inspection ID 5001
Firm Bluffton Hlth Systems LLC dba Bluffton Regional Med Ctr
FEI number 1000518089
Address Radiology Department, 303 S Main St
City Bluffton
State IN
ZIP 46714-2503
Fiscal year 2000
Inspection end date Nov 23, 1999
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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