# GlaxoSmithKline LLC, Collegeville, PA – FDA Inspections

Source: https://www.keypedia.com/companies/glaxosmithkline-llc/b0586c5b-ed04-498a-befc-515b46a93b3a

> Inspection records and compliance data for GlaxoSmithKline LLC in Collegeville, Pennsylvania. 8 FDA inspections on record, last inspected October 21, 2025.

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## Details

- Name: GlaxoSmithKline LLC
- FEI Number: 3006810568
- Address Line 1: 1250 S Collegeville Rd
- City: Collegeville
- State: Pennsylvania
- Zip Code: 19426
- Country Name: United States
- Address: 1250 S Collegeville Rd, Collegeville, Pennsylvania 19426, United States
- Country: United States

## Related Documents

- FDA Inspection 1269601 - GlaxoSmithKline LLC - 2025-10-21 — source: FDA, date: October 21, 2025
- FDA Inspection 1269601 - GlaxoSmithKline LLC - 2025-10-21 — classification: No Action Indicated (NAI), source: FDA, date: October 21, 2025
- FDA Inspection 1253764 - GlaxoSmithKline LLC - 2024-11-22 — source: FDA, date: November 22, 2024
- FDA Inspection 1253764 - GlaxoSmithKline LLC - 2024-11-22 — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2024
- FDA Inspection 1187325 - GlaxoSmithKline LLC - 2022-10-24 — classification: No Action Indicated (NAI), source: FDA, date: October 24, 2022
- FDA Inspection 1180594 - GlaxoSmithKline LLC - 2022-08-12 — classification: No Action Indicated (NAI), source: FDA, date: August 12, 2022
- FDA Inspection 886173 - GlaxoSmithKline LLC - 2014-06-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 3, 2014
- [FDA Inspection 805603 - GlaxoSmithKline LLC - 2012-11-01](https://www.keypedia.com/records/fda_inspections/glaxosmithkline-llc/6a59303c-a690-4300-8bae-39abb1bffe78) — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2012
- FDA Inspection 800384 - GlaxoSmithKline LLC - 2012-09-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 19, 2012
- FDA Inspection 556783 - GlaxoSmithKline LLC - 2009-01-16 — classification: No Action Indicated (NAI), source: FDA, date: January 16, 2009

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