FDA inspection citations: Nubratori, Inc (3 observations)
FDA cites Nubratori, Inc. for sterile drug production issues.
What changed & why it matters
Med Spa Radar recorded an FDA inspection citation at the federal level, dated December 11, 2025, 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
- December 11, 2025
What this means for your specific practice — the exact step to take, the deadline to calendar, or the supplier detail to check — is in the member "what to do" below. This page is the free record of what changed and why it matters.
Firm inspection: Voluntary Action Indicated
This firm’s most recent FDA inspection was classified Voluntary Action Indicated (VAI) — objectionable conditions FDA expects the firm to correct.
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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Monitoring, not legal advice.