# Loop Plaza Pharmacy Company DBA Loop Compounding Pharmacy - Inspection Records

Source: https://www.globalkeysolutions.net/companies/loop-plaza-pharmacy-company-dba-loop-compounding-pharmacy/0d7aab25-7237-48d8-bff0-f4bcd08bbfeb

> Inspection records and compliance data for Loop Plaza Pharmacy Company DBA Loop Compounding Pharmacy in Saint Albans, West Virginia. Access full analysis and detailed observations.

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## Details

- Name: Loop Plaza Pharmacy Company DBA Loop Compounding Pharmacy
- FEI Number: 3004610520
- City: Saint Albans
- State: West Virginia
- Country Name: United States
- Address Line 1: 72 6th Ave
- Zip Code: 25177
- Facility Type: Producer of Sterile and Non Sterile Drug Products

## Related Documents

- [483 - Loop Plaza Pharmacy Company DBA Loop Compounding Pharmacy - 2018-09-25](https://www.globalkeysolutions.net/records/483/loop-plaza-pharmacy-company-dba-loop-compounding-pharmacy/b6e52571-a039-4e36-8f59-7c15eb2ad608) — source: FDA, date: September 25, 2018
- [483 - Loop Plaza Pharmacy Company DBA Loop Compounding Pharmacy - 2018-09-25](https://www.globalkeysolutions.net/records/483/loop-plaza-pharmacy-company-dba-loop-compounding-pharmacy/b14de416-a9e6-401f-84e1-be6018f691f3) — source: FDA, date: September 25, 2018
- [WARNING_LETTER - Loop Plaza Pharmacy Company DBA Loop Compounding Pharmacy - 2016-12-16](https://www.globalkeysolutions.net/records/warning_letter/loop-plaza-pharmacy-company-dba-loop-compounding-pharmacy/e286f1e6-c562-4986-ab39-494162fd1c27) — source: FDA, date: December 16, 2016
- [483 - Loop Plaza Pharmacy Company DBA Loop Compounding Pharmacy - 2016-12-16](https://www.globalkeysolutions.net/records/483/loop-plaza-pharmacy-company-dba-loop-compounding-pharmacy/696411fc-667f-4523-85a8-b639a3930c32) — source: FDA, date: December 16, 2016
- [FDA Inspection 1003112 - Loop Plaza Pharmacy Company DBA Loop Compounding Pharmacy - 2016-12-16](https://www.globalkeysolutions.net/records/fda_inspections/loop-plaza-pharmacy-company-dba-loop-compounding-pharmacy/48a9fa9f-40c4-4196-94a3-76dc3135bcb1) — classification: Official Action Indicated (OAI), source: FDA, date: December 16, 2016

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