# Alopecil Corporation, S.R.L., Santo Domingo Oeste, Dominican Republic (the) – FDA Inspections

Source: https://www.keypedia.com/companies/alopecil-corporation-srl/d666a9b8-72e0-458c-929d-a8a8f727a1a6

> Inspection records and compliance data for Alopecil Corporation, S.R.L. in Santo Domingo Oeste. 3 FDA inspections on record (2 OAI), 1 warning letter, last inspected June 08, 2016.

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## Details

- Name: Alopecil Corporation, S.R.L.
- FEI Number: 3010098874
- Address Line 1: Haina, D.N., Autopista 30 De Mayo No. 111
- City: Santo Domingo Oeste
- Country Name: Dominican Republic (the)
- Address: Haina, D.N., Autopista 30 De Mayo No. 111, Santo Domingo Oeste, Dominican Republic (the)
- Country: Dominican Republic (the)

## Related Documents

- [FDA Inspection 976844 - Alopecil Corporation, S.R.L. - 2016-06-08](https://www.keypedia.com/records/fda_inspections/alopecil-corporation-srl/e9419282-424a-4482-a852-98984697b8ba) — classification: Official Action Indicated (OAI), source: FDA, date: June 8, 2016
- [WARNING_LETTER - Alopecil Corporation, S.R.L. - 2014-01-15](https://www.keypedia.com/records/warning_letter/alopecil-corporation-srl/a6526d91-6786-479b-87c3-faf0f04c580b) — source: FDA, date: January 15, 2014
- [FDA Inspection 864911 - Alopecil Corporation, S.R.L. - 2014-01-15](https://www.keypedia.com/records/fda_inspections/alopecil-corporation-srl/0da6abfe-a18a-4915-b000-3b54b4dd7f24) — classification: Official Action Indicated (OAI), source: FDA, date: January 15, 2014
- FDA Inspection 864911 - Alopecil Corporation, S.R.L. - 2014-01-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 15, 2014
- [FDA Inspection 810484 - Alopecil Corporation, S.R.L. - 2012-12-07](https://www.keypedia.com/records/fda_inspections/alopecil-corporation-srl/8a8e77fe-d180-496e-93ee-9a65a93a671f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 7, 2012
- FDA Inspection 810484 - Alopecil Corporation, S.R.L. - 2012-12-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 7, 2012

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