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FDA Form 483 – API Manufacturing Facility (CTO-2)
FDA Form 483 – API Manufacturing Facility (CTO-2)
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$69.00 USD
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Original Request: USFDA completed a GMP inspection at API manufacturing facility (CTO-2) in Bollaram, Hyderabad. The inspection was conducted from 13th November, 2024 to 19th November, 2024. company has been issued a Form 483 with 7 observations. We need copy of those records
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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