FDA inspection citations: Tan-Alize Kozmetik ve Temizlik Urunleri Sanayi ve Ticaret A.S. (7 observations)
FDA inspection reveals quality concerns for a facility supplying med spas.
What changed & why it matters
MedSpaRadar recorded an FDA inspection citation at the federal level, dated February 27, 2026, in the GLP-1 Compounding category.
An inspection citation records what FDA investigators observed at a drug or biologic facility. For an aesthetic practice, the question a citation raises is supplier due-diligence: a cited compounder or outsourcing facility is one whose FDA inspection history is now on the public record.
- Type
- FDA Inspection Citation
- Jurisdiction
- Federal
- Category
- GLP-1 Compounding
- Recorded
- February 27, 2026
What this means for your practice — the step to take, the deadline to calendar or the supplier detail to check, where the change calls for one — is in the member "what to do" below. This page is the free record of what changed and why it matters.
Firm inspection: Official Action Indicated
This firm’s most recent FDA inspection was classified Official Action Indicated (OAI) — FDA’s most serious outcome, signaling significant violations.
Source: FDA Data Dashboard inspection classifications (most recent, by firm FEI).
What to do
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FDA Inspection Citation · primary source ↗
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MedSpaRadar is regulatory monitoring and reference: it summarizes public laws, regulations and agency actions and links each to its source. It is not legal, medical, or compliance advice, and using it creates no attorney-client relationship. A summary can lag its source or leave out detail, and monitoring itself can be interrupted — so an absence of alerts means nothing reached you, not that nothing happened. Read the cited source, check its effective date, and confirm any change to your operations or clinical practice with qualified health-law counsel and your medical director.