# Nutricia North America, Rockville, MD – FDA Inspections

Source: https://www.keypedia.com/companies/nutricia-north-america/0c965344-1c01-4cf7-8dda-7e02afb5c84f

> Inspection records and compliance data for Nutricia North America in Rockville, Maryland. 8 FDA inspections on record, last inspected January 30, 2024.

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## Details

- Name: Nutricia North America
- FEI Number: 1122128
- Address Line 1: 77 Upper Rock Cir Ste 303
- City: Rockville
- State: Maryland
- Zip Code: 20850
- Country Name: United States
- Address: 77 Upper Rock Cir Ste 303, Rockville, Maryland 20850, United States
- Country: United States

## Related Documents

- FDA Inspection 1228985 - Nutricia North America - 2024-01-30 — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2024
- FDA Inspection 1122992 - Nutricia North America - 2020-02-11 — classification: No Action Indicated (NAI), source: FDA, date: February 11, 2020
- FDA Inspection 1122992 - Nutricia North America - 2020-02-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 11, 2020
- FDA Inspection 1018162 - Nutricia North America - 2017-07-07 — classification: No Action Indicated (NAI), source: FDA, date: July 7, 2017
- FDA Inspection 802985 - Nutricia North America - 2012-10-11 — classification: No Action Indicated (NAI), source: FDA, date: October 11, 2012
- FDA Inspection 757176 - Nutricia North America - 2011-12-02 — classification: No Action Indicated (NAI), source: FDA, date: December 2, 2011
- FDA Inspection 757176 - Nutricia North America - 2011-12-02 — classification: No Action Indicated (NAI), source: FDA, date: December 2, 2011
- FDA Inspection 696903 - Nutricia North America - 2010-11-08 — classification: No Action Indicated (NAI), source: FDA, date: November 8, 2010
- FDA Inspection 696903 - Nutricia North America - 2010-11-08 — classification: No Action Indicated (NAI), source: FDA, date: November 8, 2010
- FDA Inspection 660148 - Nutricia North America - 2010-04-29 — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2010

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